Drugs

Extended Use Dates Provided by Pfizer

Extended Use Dates to Assist with Sterile Water for Injection (small-volume vials in 10 mL, 20 mL, 50 mL and 100 mL presentations) Manufactured Intermittent Supply Interruptions

[October 11, 2018] Due to the intermittent supply interruptions of sterile water for  injection, FDA is alerting health care professionals and patients of updated dates through which some sterile water for injection, manufactured by Hospira, a Pfizer company, may be used beyond the manufacturer’s labeled expiration date. To help ensure patient safety, these products should have been — and should continue to be — stored as labeled.

Based on stability data provided by Pfizer and reviewed by FDA, the following extended use dates are supported for specific batches indicated in the tables below. Patients that have the batch numbers below will be able to use them through the corresponding new use dates to help with supply. As data become available, this list can continue to expand.

FDA is not requiring or recommending that the identified batches in the following tables be relabeled with their new use dates. However, if replacement product becomes available during the extension period, then the agency expects the lots in these tables will be replaced and properly disposed of as soon as possible.

Please see the recent FDA in Brief for more information, and contact CDER Drug Shortage Staff at drugshortages@fda.hhs.gov with questions regarding these tables.

NDC NumberLOT #EXP. DATENEW EXP. DATE
00409-4887-10580074P1-Oct-181-Oct-19
00409-4887-10580084P1-Oct-181-Oct-19
00409-4887-10580094P1-Oct-181-Oct-19
00409-4887-10600104P1-Dec-181-Dec-19
00409-4887-10610104P1-Jan-191-Jan-20
00409-4887-10610124P1-Jan-191-Jan-20
00409-4887-10630034P1-Feb-191-Feb-20
00409-4887-10640064P1-Feb-191-Feb-20
00409-4887-20640174P1-Feb-191-Feb-20
00409-4887-20650214P1-Feb-191-Feb-20
00409-4887-10630044P1-Mar-191-Mar-20
00409-4887-10630064P1-Mar-191-Mar-20
00409-4887-10630104P1-Mar-191-Mar-20
00409-4887-10630154P1-Mar-191-Mar-20
00409-4887-10630144P1-Mar-191-Mar-20
00409-4887-10640014P1-Mar-191-Mar-20
00409-4887-10640054P1-Mar-191-Mar-20
00409-4887-10640074P1-Mar-191-Mar-20
00409-4887-2058427DK10/1/201810/1/2019
00409-4887-5058400DK10/1/201810/1/2019
00409-4887-5058401DK10/1/201810/1/2019
00409-4887-5058402DK10/1/201810/1/2019
00409-4887-5058403DK10/1/201810/1/2019
00409-4887-5058408DK10/1/201810/1/2019
00409-4887-1058157DK10/1/201810/1/2019
00409-4887-1058158DK10/1/201810/1/2019
00409-4887-1058159DK10/1/201810/1/2019
00409-4887-1058160DK10/1/201810/1/2019
00409-4887-1058246DK10/1/201810/1/2019
00409-4887-1058247DK10/1/201810/1/2019
00409-4887-1058250DK10/1/201810/1/2019
00409-4887-1058442DK10/1/201810/1/2019
00409-4887-2059002DK11/1/201811/1/2019
00409-4887-2059003DK11/1/201811/1/2019
00409-4887-2059102DK11/1/201811/1/2019
00409-4887-2059419DK11/1/201811/1/2019
00409-4887-2059420DK11/1/201811/1/2019
00409-4887-1059012DK11/1/201811/1/2019
00409-4887-1059013DK11/1/201811/1/2019
00409-4887-1059319DK11/1/201811/1/2019
00409-4887-1059349DK11/1/201811/1/2019
00409-4887-1059350DK11/1/201811/1/2019
00409-4887-1059351DK11/1/201811/1/2019
00409-4887-1059378DK11/1/201811/1/2019
00409-4887-1059379DK11/1/201811/1/2019
00409-4887-1059380DK11/1/201811/1/2019
00409-4887-1059381DK11/1/201811/1/2019
00409-4887-2060054DK12/1/201812/1/2019
00409-4887-2060055DK12/1/201812/1/2019
00409-4887-2060056DK12/1/201812/1/2019
00409-4887-1060015DK12/1/201812/1/2019
00409-4887-1060016DK12/1/201812/1/2019
00409-4887-2061005DK1/1/20191/1/2020
00409-4887-2061006DK1/1/20191/1/2020
00409-4887-2061007DK1/1/20191/1/2020
00409-4887-2061008DK1/1/20191/1/2020
00409-4887-2061010DK1/1/20191/1/2020
00409-4887-2061299DK1/1/20191/1/2020
00409-4887-2061366DK1/1/20191/1/2020
00409-4887-2061368DK1/1/20191/1/2020
00409-4887-5061099DK1/1/20191/1/2020
00409-4887-5061363DK1/1/20191/1/2020
00409-4887-9961276DK1/1/20191/1/2020
00409-4887-9961279DK1/1/20191/1/2020
00409-4887-9961280DK1/1/20191/1/2020
00409-4887-1061062DK1/1/20191/1/2020
00409-4887-1061063DK1/1/20191/1/2020
00409-4887-1061064DK1/1/20191/1/2020
00409-4887-2062018DK2/1/20192/2/2020
00409-4887-2062019DK2/1/20192/2/2020
00409-4887-2062418DK2/1/20192/2/2020
00409-4887-5062290DK2/1/20192/2/2020
00409-4887-9962316DK2/1/20192/2/2020
00409-4887-9962317DK2/1/20192/2/2020
00409-4887-9962318DK2/1/20192/2/2020
00409-4887-9962319DK2/1/20192/2/2020
00409-4887-1062228DK2/1/20192/2/2020
00409-4887-1062229DK2/1/20192/2/2020
00409-4887-1062230DK2/1/20192/2/2020
00409-4887-2063443DK3/1/20193/1/2020
00409-4887-2063444DK3/1/20193/1/2020
00409-4887-2063445DK3/1/20193/1/2020
00409-4887-2063446DK3/1/20193/1/2020
00409-4887-5063278DK3/1/20193/1/2020
00409-4887-5063279DK3/1/20193/1/2020
00409-4887-5063280DK3/1/20193/1/2020
00409-4887-5063462DK3/1/20193/1/2020
00409-4887-5063463DK3/1/20193/1/2020
00409-4887-9963170DK3/1/20193/1/2020
00409-4887-9963425DK3/1/20193/1/2020
00409-4887-9963426DK3/1/20193/1/2020

Extended Use Dates to Assist with Sodium Bicarbonate Injection Shortage

[September 27, 2018] This is to update the information posted here previously on 6/15/17, 6/23/17, 7/19/17, 8/17/17, 11/9/2017, and 6/12/2018. Due to the ongoing critical shortage of injectable drugs used in critical care, FDA is alerting health care professionals and emergency responders of updated dates through which some of these injectable drugs, manufactured by Hospira Inc, a Pfizer company, may be used beyond the manufacturer’s labeled expiration date. To help ensure patient safety, these products should have been — and should continue to be — stored as labeled. 

Based on stability data provided by Pfizer and reviewed by FDA, the tables of specific lots with extended use dates have been updated for the following products:

  • Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-02)
  • Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-25) LABELLED AS NOVAPLUS

Hospitals that have the following lot numbers in stock will be able to use them through the corresponding new use dates to help with supply. As data become available, this list can continue to expand.

FDA is not requiring or recommending that the identified lots in the following tables be relabeled with their new use dates. However, if replacement product becomes available during the extension period, then it is expected that the lots in these tables will be replaced and properly disposed of as soon as possible.

Please contact CDER Drug Shortage Staff at drugshortages@fda.hhs.gov with questions regarding these tables.

Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-02)

Product/
Lot Number

Manufacturer’s Original         
Expiry Date

New Use Date
(beyond manufacturer’s original expiry date)

65197EV

1-May-2018

1-Oct-2018

65200EV

1-May-2018

1-Oct-2018

65205EV

1-May-2018

1-Oct-2018

65206EV

1-May-2018

1-Oct-2018

65503EV

1-May-2018

1-Oct-2018

65504EV

1-May-2018

1-Oct-2018

67138EV

1-Jul-2018

1-Dec-2018

67139EV

1-Jul-2018

1-Dec-2018

67140EV

1-Jul-2018

1-Dec-2018

67141EV

1-Jul-2018

1-Dec-2018

67142EV

1-Jul-2018

1-Dec-2018

67248EV

1-Jul-2018

1-Dec-2018

67279EV

1-Jul-2018

1-Dec-2018

67280EV

1-Jul-2018

1-Dec-2018

67281EV

1-Jul-2018

1-Dec-2018

67282EV

1-Jul-2018

1-Dec-2018

67283EV

1-Jul-2018

1-Dec-2018

67284EV

1-Jul-2018

1-Dec-2018

68059EV

1-Aug-2018

1-Jan-2019

68192EV

1-Aug-2018

1-Jan-2019

68193EV

1-Aug-2018

1-Jan-2019

68194EV

1-Aug-2018

1-Jan-2019

68308EV

1-Aug-2018

1-Jan-2019

68309EV

1-Aug-2018

1-Jan-2019

68429EV

1-Aug-2018

1-Jan-2019

68430EV

1-Aug-2018

1-Jan-2019

68431EV

1-Aug-2018

1-Jan-2019

69006EV

1-Sep-2018

1-Feb-2019

69008EV

1-Sep-2018

1-Feb-2019

69180EV

1-Sep-2018

1-Feb-2019

69181EV

1-Sep-2018

1-Feb-2019

69182EV

1-Sep-2018

1-Feb-2019

69353EV

1-Sep-2018

1-Feb-2019

69354EV

1-Sep-2018

1-Feb-2019

69355EV

1-Sep-2018

1-Feb-2019

69356EV

1-Sep-2018

1-Feb-2019

69357EV

1-Sep-2018

1-Feb-2019

69358EV

1-Sep-2018

1-Feb-2019

69361EV

1-Sep-2018

1-Feb-2019

69362EV

1-Sep-2018

1-Feb-2019

69376EV

1-Sep-2018

1-Feb-2019

69379EV

1-Sep-2018

1-Feb-2019

69380EV

1-Sep-2018

1-Feb-2019

70143EV

1-Oct-2018

1-Mar-2019

70316EV

1-Oct-2018

1-Mar-2019

70317EV

1-Oct-2018

1-Mar-2019

70318EV

1-Oct-2018

1-Mar-2019

71055EV

1-Nov-2018

1-Apr-2019

71056EV

1-Nov-2018

1-Apr-2019

71058EV

1-Nov-2018

1-Apr-2019

71079EV

1-Nov-2018

1-Apr-2019

71080EV

1-Nov-2018

1-Apr-2019

71081EV

1-Nov-2018

1-Apr-2019

71154EV

1-Nov-2018

1-Apr-2019

71339EV

1-Nov-2018

1-Apr-2019

Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-25) LABELLED AS NOVAPLUS

Product/
Lot Number

Manufacturer’s Original
Expiry Date

New Use Date
(beyond manufacturer’s original expiry date)

70064EV

1-Oct-2018

1-Mar-2019

70186EV

1-Oct-2018

1-Mar-2019

70255EV

1-Oct-2018

1-Mar-2019

71110EV

1-Nov-2018

1-Apr-2019

Extended use dates to assist with Aminophylline injection intermittent supply interruptions

[Sept 12, 2018] Due to the intermittent supply interruptions of Aminophylline injection, FDA is alerting health care professionals and patients of updated dates through which some Aminophylline injection, manufactured by Hospira, a Pfizer company, may be used beyond the manufacturer’s labeled expiration date. To help ensure patient safety, these products should have been — and should continue to be — stored as labeled.

Based on stability data provided by Pfizer and reviewed by FDA, the following extended use dates are supported for specific batches indicated in the tables below. Patients that have the batch numbers below will be able to use them through the corresponding new use dates to help with supply. As data become available, this list can continue to expand.

FDA is not requiring or recommending that the identified batches in the following tables be relabeled with their new use dates. However, if replacement product becomes available during the extension period, then the agency expects the lots in these tables will be replaced and properly disposed of as soon as possible.

Please see the recent FDA in Brief for more information, and contact CDER Drug Shortage Staff at drugshortages@fda.hhs.gov with questions regarding these tables.

NDC NUMBERLOT #MFG. DATEEXP DATENEW EXP DATE
00409-5921-0176328DK4/12/201710/1/20182/1/2019
00409-5921-0176329DK4/13/201710/1/20182/1/2019
00409-5921-0176330DK4/17/201710/1/20182/1/2019
00409-5922-0176331DK4/18/201710/1/20182/1/2019

Extended use dates to assist with EpiPen intermittent supply interruptions

[August 21, 2018] Due to the intermittent supply interruptions of EpiPen, FDA is alerting health care professionals and patients of updated dates through which some EpiPens and the authorized generic version, manufactured by Meridian Medical Technologies, a Pfizer company, may be used beyond the manufacturer’s labeled expiration date. To help ensure patient safety, these products should have been—and should continue to be—stored as labeled.

Based on stability data provided by Pfizer and reviewed by FDA, the following extended use dates are supported for specific batches indicated in the tables below. Patients that have the batch numbers below will be able to use them through the corresponding new use dates to help with supply. As data become available, this list can continue to expand.

FDA is not requiring or recommending that the identified batches in the following tables be relabeled with their new use dates. However, if replacement product becomes available during the extension period, then the agency expects the lots in these tables will be replaced and properly disposed of as soon as possible.

Please see the recent FDA in Brief for more information, and contact CDER Drug Shortage Staff at drugshortages@fda.hhs.gov with questions regarding these tables.

Epinephrine Injection, USP 0.3 mg Auto-Injectors
NDC 49502-102-02 appears on the box
NDC 49502-102-01 appears on the individual device within the box

BatchManufacturer's Original
Expiration Date
New Expiration Date
(beyond manufacturer's
original expiry date)
6FM7224/20188/2018
6FM7394/20188/2018
6FM7714/20188/2018
6FM7724/20188/2018
6FM7734/20188/2018
6FM7155/20189/2018
6FM7165/20189/2018
6FM7565/20189/2018
6FM7575/20189/2018
6FM7685/20189/2018
6FM7805/20189/2018
6FM7815/20189/2018
6FM7825/20189/2018
6FM7835/20189/2018
6FM7856/201810/2018
6FM7876/201810/2018
7FM1158/201812/2018
7FM1178/201812/2018
7FM1208/201812/2018
7FM1348/201812/2018
7FM1749/20181/2019
7FM1759/20181/2019
7FM27410/20182/2019
7FM27510/20182/2019
7FM27610/20182/2019

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EpiPen® (epinephrine injection, USP) 0.3 mg Auto-Injectors
NDC 49502-500-02 appears on the box
NDC 49502-500-01 appears on the individual device within the box
 

BatchManufacturer's Original
Expiration Date
New Expiration Date
(beyond manufacturer's
original expiry date)
6GM4804/20188/2018
6GM4814/20188/2018
6GM5034/20188/2018
6GM5044/20188/2018
6GM5064/20188/2018
6GM5074/20188/2018
6GM5124/20188/2018
6GM6694/20188/2018
6GM5995/20189/2018
6GM6856/201810/2018
6GM7666/201810/2018
6GM7676/201810/2018
7GM0268/201812/2018
7GM0458/201812/2018
7GM0489/20181/2019
7GM0549/20181/2019
7GM1649/20181/2019
7GM1729/20181/2019
7GM1739/20181/2019
7GM2729/20181/2019
7GM19110/20182/2019
7GM20011/20183/2019
7GM20111/20183/2019
7GM20312/20184/2019
7GM20412/20184/2019
7GM21212/20184/2019
7GM21312/20184/2019
7GM36012/20184/2019
7GM36112/20184/2019

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Extended use dates to assist with emergency syringe shortages

[June 12, 2018] This is to update and consolidate the information posted here previously on 6/15/17, 6/23/17, 7/19/17, 8/17/17, and 11/9/2017. Due to the ongoing critical shortage of injectable drugs used in critical care, FDA is alerting health care professionals and emergency responders of updated dates through which some of these injectable drugs, manufactured by Hospira Inc, a Pfizer company, may be used beyond the manufacturer’s labeled expiration date. To help ensure patient safety, these products should have been — and should continue to be — stored as labeled. 

Based on stability data provided by Pfizer and reviewed by FDA, the following extended use dates are supported for specific lots indicated in the table below for the following products:

  • Atropine Sulfate Injection, USP 0.1 mg/mL; 5 mL Abboject syringe (NDC 0409-4910-34)
  • Atropine Sulfate Injection, USP 0.1 mg/mL; 10 mL Abboject syringe (NDC 0409-4911-34)
  • Atropine Sulfate Injection, USP 0.1 mg/mL; 10 mL Ansyr Plastic syringe (NDC 0409-1630-10)
  • Dextrose injection, USP 50% (0.5 g/mL); 25 g/50 mL Abboject syringe (NDC 0409-4902-34)
  • Dextrose injection, USP 50% (0.5 g/mL); 25 g/50 mL Ansyr Plastic Syringe (NDC 0409-7517-16)
  • Epinephrine Injection, USP 0.1 mg/mL; 10 mL Abboject syringe (NDC 0409-4921-34) (bundle of 10 syringes) and NDC 0409-4921-20 (1 syringe)
  • Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Abboject Glass Syringe (18 G x 1 ½" needle) (NDC 0409-6637-34)
  • Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-02)
  • Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-25) LABELLED AS NOVAPLUS

Hospitals that have the following lot numbers in stock will be able to use them through the corresponding new use dates to help with supply. As data become available, this list can continue to expand.

FDA is not requiring or recommending that the identified lots in the following tables be relabeled with their new use dates. However, if replacement product becomes available during the extension period, then it is expected that the lots in these tables will be replaced and properly disposed of as soon as possible.

Further information is here. Please contact CDER Drug Shortage Staff at drugshortages@fda.hhs.gov with questions regarding these tables.

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Atropine Sulfate Injection, USP 0.1 mg/mL; 5 mL ABBOJECT syringe (NDC 0409-4910-34)

Product/
Lot Number
Manufacturer’s Original         
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
63183DK001-Mar-20181-Sep-2018
64293DK001-Apr-20181-Oct-2018
67331DK001-Jul-20181-Jan-2019
69292DK001-Sep-20181-Mar-2019

 

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Atropine Sulfate Injection, USP 0.1 mg/mL; 10 mL ABBOJECT syringe (NDC 0409-4911-34)

Product/
Lot Number
Manufacturer’s Original         
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
56053DK001-Aug-20171-Aug-2018
57032DK001-Sep-20171-Sep-2018
57033DK001-Sep-20171-Sep-2018
57034DK001-Sep-20171-Sep-2018
57035DK001-Sep-20171-Sep-2018
58004DK001-Oct-20171-Oct-2018
58006DK001-Oct-20171-Oct-2018
58007DK001-Oct-20171-Oct-2018
58424DK001-Oct-20171-Oct-2018
58425DK001-Oct-20171-Oct-2018
59039DK001-Nov-20171-Nov-2018
59051DK001-Nov-20171-Nov-2018
59052DK001-Nov-20171-Nov-2018
59384DK001-Nov-20171-Nov-2018
62470DK001-Feb-20181-Feb-2019
63292DK001-Mar-20181-Mar-2019
63293DK001-Mar-20181-Mar-2019
63318DK001-Mar-20181-Mar-2019
63319DK001-Mar-20181-Mar-2019
64271DK001-Apr-20181-Apr-2019
64301DK001-Apr-20181-Apr-2019
64302DK001-Apr-20181-Apr-2019
65255DK001-May-20181-May-2019
66267DK001-Jun-20181-Jun-2019
67259DK001-Jul-20181-Jul-2019
67302DK001-Jul-20181-Jul-2019
71343DK00 1-Nov-2018 1-Nov-2019

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Atropine Sulfate Injection, USP 0.1 mg/mL; 10 mL Ansyr Plastic syringe (NDC 0409-1630-10)

Product/
Lot Number
Manufacturer’s Original         
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
62292EV001-Feb-20181-Aug-2018
62294EV001-Feb-20181-Aug-2018
68327EV001-Aug-20181-Feb-2019
68328EV001-Aug-20181-Feb-2019
68439EV001-Aug-20181-Feb-2019
68440EV001-Aug-20181-Feb-2019
70046EV001-Oct-20181-Apr-2019
70047EV001-Oct-20181-Apr-2019
70048EV001-Oct-20181-Apr-2019
70049EV001-Oct-20181-Apr-2019
71130EV001-Nov-20181-May-2019
71197EV001-Nov-20181-May-2019
71319EV001-Nov-20181-May-2019

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Dextrose 50% Injection, USP, 50 mL ABBOJECT Syringe (NDC 0409-4902-34)

Product/
Lot Number
Manufacturer’s Original         
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
55177DK001-Jul-20171-Jul-2018
55178DK001-Jul-20171-Jul-2018
56025DK001-Aug-20171-Aug-2018
56160DK001-Aug-20171-Aug-2018
56162DK001-Aug-20171-Aug-2018
58131DK001-Oct-20171-Oct-2018
59027DK001-Nov-20171-Nov-2018
63391DK001-Mar-20181-Mar-2019
63392DK001-Mar-20181-Mar-2019
63475DK001-Mar-20181-Mar-2019
64278DK001-Apr-20181-Apr-2019
64282DK001-Apr-20181-Apr-2019
65468DK001-May-20181-May-2019
66007DK001-Jun-20181-Jun-2019
66387DK001-Jun-20181-Jun-2019
67040DK001-Jul-20181-Jul-2019
67041DK001-Jul-20181-Jul-2019
67042DK001-Jul-20181-Jul-2019
68082DK001-Aug-2018 1-Aug-2019
68458DK001-Aug-2018 1-Aug-2019

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Dextrose injection 50% (0.5 g/mL); 25 g/50 mL Ansyr Plastic Syringe (NDC 0409-7517-16)

Product/
Lot Number
Manufacturer’s Original         
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
61036EV001-Jan-20181-Jul-2018
61037EV001-Jan-20181-Jul-2018
61038EV001-Jan-20181-Jul-2018
61103EV001-Jan-20181-Jul-2018
61201EV001-Jan-20181-Jul-2018
61318EV001-Jan-20181-Jul-2018
61319EV001-Jan-20181-Jul-2018
61320EV001-Jan-20181-Jul-2018
62094EV001-Feb-20181-Aug-2018
62095EV001-Feb-20181-Aug-2018
62096EV001-Feb-20181-Aug-2018
62097EV001-Feb-20181-Aug-2018
63023EV001-Mar-20181-Sep-2018
63024EV001-Mar-20181-Sep-2018
63025EV001-Mar-20181-Sep-2018
63119EV001-Mar-20181-Sep-2018
63490EV001-Mar-20181-Sep-2018
63491EV001-Mar-20181-Sep-2018
63492EV001-Mar-20181-Sep-2018
63493EV001-Mar-20181-Sep-2018
64333EV001-Apr-20181-Oct-2018
64334EV001-Apr-20181-Oct-2018
64335EV001-Apr-20181-Oct-2018
65411EV001-May-20181-Nov-2018
65413EV001-May-20181-Nov-2018
65482EV001-May-20181-Nov-2018
65483EV001-May-20181-Nov-2018
66203EV001-Jun-20181-Dec-2018
66204EV001-Jun-20181-Dec-2018
66205EV001-Jun-20181-Dec-2018
67171EV001-Jul-20181-Jan-2019
67329EV001-Jul-20181-Jan-2019
68009EV001-Aug-20181-Feb-2019
68010EV001-Aug-20181-Feb-2019
68011EV001-Aug-20181-Feb-2019
68187EV001-Aug-20181-Feb-2019
68188EV001-Aug-20181-Feb-2019
68189EV001-Aug-20181-Feb-2019
68190EV001-Aug-20181-Feb-2019
69098EV001-Sep-20181-Mar-2019
69099EV001-Sep-20181-Mar-2019
69100EV001-Sep-20181-Mar-2019
69101EV001-Sep-20181-Mar-2019
69102EV001-Sep-20181-Mar-2019
69188EV001-Sep-20181-Mar-2019
69189EV001-Sep-20181-Mar-2019
69190EV001-Sep-20181-Mar-2019
69191EV001-Sep-20181-Mar-2019
69192EV001-Sep-20181-Mar-2019
70189EV001-Oct-20181-Apr-2019
70190EV001-Oct-20181-Apr-2019
70191EV001-Oct-20181-Apr-2019
70192EV001-Oct-20181-Apr-2019
71190EV001-Nov-20181-May-2019
71191EV001-Nov-20181-May-2019
71192EV001-Nov-20181-May-2019
71193EV001-Nov-20181-May-2019
71323EV001-Nov-20181-May-2019
71324EV001-Nov-20181-May-2019
71325EV001-Nov-20181-May-2019
71326EV001-Nov-20181-May-2019
72102EV001-Dec-20181-Jun-2019
72103EV001-Dec-20181-Jun-2019
72104EV001-Dec-20181-Jun-2019
72105EV001-Dec-20181-Jun-2019
73059EV001-Jan-20191-Jul-2019
73060EV001-Jan-20191-Jul-2019
73061EV001-Jan-20191-Jul-2019
73062EV001-Jan-20191-Jul-2019
73140EV001-Jan-20191-Jul-2019

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Epinephrine Injection, USP 0.1 mg/mL; 10 mL ABBOJECT syringe (NDC 0409-4921-34) (bundle of 10 syringes) and (NDC 0409-4921-20) (1 syringe)

Product/
Lot Number
Manufacturer’s Original
Expiry Date
New Use Date
(beyond manufacturer’s original expiry date)
62359DK001-Nov-20171-Aug-2018
62360DK001-Nov-20171-Aug-2018
62404DK001-Nov-20171-Aug-2018
62405DK001-Nov-20171-Aug-2018
62406DK001-Nov-20171-Aug-2018
62407DK001-Nov-20171-Aug-2018
62409DK001-Nov-20171-Aug-2018
62414DK001-Nov-20171-Aug-2018
62415DK001-Nov-20171-Aug-2018
62416DK001-Nov-20171-Aug-2018
62417DK001-Nov-20171-Aug-2018
62447DK001-Nov-20171-Aug-2018
62485DK001-Nov-20171-Aug-2018
63161DK001-Dec-20171-Sep-2018
63162DK001-Dec-20171-Sep-2018
63163DK001-Dec-20171-Sep-2018
63164DK001-Dec-20171-Sep-2018
63173DK001-Dec-20171-Sep-2018
63175DK001-Dec-20171-Sep-2018
63180DK001-Dec-20171-Sep-2018
63263DK001-Dec-20171-Sep-2018
63264DK001-Dec-20171-Sep-2018
63265DK001-Dec-20171-Sep-2018
63266DK001-Dec-20171-Sep-2018
63267DK001-Dec-20171-Sep-2018
63294DK001-Dec-20171-Sep-2018
63295DK001-Dec-20171-Sep-2018
63296DK001-Dec-20171-Sep-2018
63297DK001-Dec-20171-Sep-2018
63393DK001-Dec-20171-Sep-2018
64268DK001-Jan-20181-Oct-2018
64269DK001-Jan-20181-Oct-2018
64270DK001-Jan-20181-Oct-2018
64294DK001-Jan-20181-Oct-2018
64295DK001-Jan-20181-Oct-2018
64296DK001-Jan-20181-Oct-2018
64303DK001-Jan-20181-Oct-2018
64304DK001-Jan-20181-Oct-2018
64305DK001-Jan-20181-Oct-2018
64307DK001-Jan-20181-Oct-2018
64308DK001-Jan-20181-Oct-2018
64309DK001-Jan-20181-Oct-2018
65054DK001-Feb-20181-Nov-2018
65068DK001-Feb-20181-Nov-2018
65069DK001-Feb-20181-Nov-2018
65070DK001-Feb-20181-Nov-2018
65244DK001-Feb-20181-Nov-2018
65245DK001-Feb-20181-Nov-2018
65246DK001-Feb-20181-Nov-2018
65248DK001-Feb-20181-Nov-2018
65249DK001-Feb-20181-Nov-2018
65250DK001-Feb-20181-Nov-2018
65251DK001-Feb-20181-Nov-2018
65252DK001-Feb-20181-Nov-2018
66010DK001-Mar-20181-Dec-2018
66011DK001-Mar-20181-Dec-2018
66056DK001-Mar-20181-Dec-2018
66130DK001-Mar-20181-Dec-2018
66155DK001-Mar-20181-Dec-2018
66157DK001-Mar-20181-Dec-2018
66161DK001-Mar-20181-Dec-2018
66162DK001-Mar-20181-Dec-2018
66250DK001-Mar-20181-Dec-2018
66253DK001-Mar-20181-Dec-2018
66264DK001-Mar-20181-Dec-2018
67016DK001-Apr-20181-Jan-2019
67075DK001-Apr-20181-Jan-2019
67076DK001-Apr-20181-Jan-2019
67078DK001-Apr-20181-Jan-2019
67079DK001-Apr-20181-Jan-2019
67080DK001-Apr-20181-Jan-2019
67081DK001-Apr-20181-Jan-2019
67085DK001-Apr-20181-Jan-2019
67086DK001-Apr-20181-Jan-2019
67087DK001-Apr-20181-Jan-2019
67088DK001-Apr-20181-Jan-2019
68086DK001-May-20181-Feb-2019
68087DK001-May-20181-Feb-2019
68090DK001-May-20181-Feb-2019
68091DK001-May-20181-Feb-2019
68092DK001-May-20181-Feb-2019
68094DK001-May-20181-Feb-2019
68096DK001-May-20181-Feb-2019
68097DK001-May-20181-Feb-2019
68098DK001-May-20181-Feb-2019
68155DK001-May-20181-Feb-2019
68156DK001-May-20181-Feb-2019
68316DK001-May-20181-Feb-2019
68317DK001-May-20181-Feb-2019
68398DK001-May-20181-Feb-2019
69171DK001-Jun-20181-Mar-2019
69172DK001-Jun-20181-Mar-2019
69273DK001-Jun-20181-Mar-2019
69274DK001-Jun-20181-Mar-2019
69278DK001-Jun-20181-Mar-2019
70265DK001-Jul-20181-Apr-2019
76158DK001-Jan-20191-Oct-2019
76159DK001-Jan-20191-Oct-2019

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Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Abboject Glass Syringe (18 G x 1 ½" needle (NDC 0409-6637-34))

Product/
Lot Number

Manufacturer’s Original         
Expiry Date

New Use Date
(beyond manufacturer’s original expiry date)

62429DK00

1-Feb-2018

1-Aug-2018

62430DK00

1-Feb-2018

1-Aug-2018

62431DK00

1-Feb-2018

1-Aug-2018

62432DK00

1-Feb-2018

1-Aug-2018

62433DK00

1-Feb-2018

1-Aug-2018

62481DK00

1-Feb-2018

1-Aug-2018

62483DK00

1-Feb-2018

1-Aug-2018

63176DK00

1-Mar-2018

1-Sep-2018

63281DK00

1-Mar-2018

1-Sep-2018

63282DK00

1-Mar-2018

1-Sep-2018

63283DK00

1-Mar-2018

1-Sep-2018

63284DK00

1-Mar-2018

1-Sep-2018

63285DK00

1-Mar-2018

1-Sep-2018

63286DK00

1-Mar-2018

1-Sep-2018

63506DK00

1-Mar-2018

1-Sep-2018

63507DK00

1-Mar-2018

1-Sep-2018

64273DK00

1-Apr-2018

1-Oct-2018

64274DK00

1-Apr-2018

1-Oct-2018

64275DK00

1-Apr-2018

1-Oct-2018

64283DK00

1-Apr-2018

1-Oct-2018

64284DK00

1-Apr-2018

1-Oct-2018

64285DK00

1-Apr-2018

1-Oct-2018

64286DK00

1-Apr-2018

1-Oct-2018

64427DK00

1-Apr-2018

1-Oct-2018

65055DK00

1-May-2018

1-Nov-2018

65056DK00

1-May-2018

1-Nov-2018

65057DK00

1-May-2018

1-Nov-2018

65060DK00

1-May-2018

1-Nov-2018

65061DK00

1-May-2018

1-Nov-2018

65062DK00

1-May-2018

1-Nov-2018

65229DK00

1-May-2018

1-Nov-2018

65230DK00

1-May-2018

1-Nov-2018

65234DK00

1-May-2018

1-Nov-2018

65235DK00

1-May-2018

1-Nov-2018

65241DK00

1-May-2018

1-Nov-2018

66004DK00

1-Jun-2018

1-Dec-2018

66005DK00

1-Jun-2018

1-Dec-2018

66006DK00

1-Jun-2018

1-Dec-2018

66054DK00

1-Jun-2018

1-Dec-2018

66055DK00

1-Jun-2018

1-Dec-2018

66127DK00

1-Jun-2018

1-Dec-2018

66128DK00

1-Jun-2018

1-Dec-2018

66389DK00

1-Jun-2018

1-Dec-2018

67045DK00

1-Jul-2018

1-Jan-2019

67046DK00

1-Jul-2018

1-Jan-2019

67047DK00

1-Jul-2018

1-Jan-2019

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Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-02)

Product/
Lot Number

Manufacturer’s Original         
Expiry Date

New Use Date
(beyond manufacturer’s original expiry date)

62052EV00

1-Feb-2018

1-Jul-2018

62053EV00

1-Feb-2018

1-Jul-2018

62093EV00

1-Feb-2018

1-Jul-2018

62132EV00

1-Feb-2018

1-Jul-2018

62133EV00

1-Feb-2018

1-Jul-2018

62134EV00

1-Feb-2018

1-Jul-2018

62135EV00

1-Feb-2018

1-Jul-2018

62181EV00

1-Feb-2018

1-Jul-2018

62182EV00

1-Feb-2018

1-Jul-2018

62183EV00

1-Feb-2018

1-Jul-2018

62184EV00

1-Feb-2018

1-Jul-2018

62185EV00

1-Feb-2018

1-Jul-2018

62208EV00

1-Feb-2018

1-Jul-2018

62209EV00

1-Feb-2018

1-Jul-2018

62210EV00

1-Feb-2018

1-Jul-2018

62212EV00

1-Feb-2018

1-Jul-2018

62213EV00

1-Feb-2018

1-Jul-2018

62232EV00

1-Feb-2018

1-Jul-2018

62454EV00

1-Feb-2018

1-Jul-2018

62456EV00

1-Feb-2018

1-Jul-2018

62457EV00

1-Feb-2018

1-Jul-2018

63027EV00

1-Mar-2018

1-Aug-2018

63028EV00

1-Mar-2018

1-Aug-2018

63029EV00

1-Mar-2018

1-Aug-2018

63030EV00

1-Mar-2018

1-Aug-2018

63031EV00

1-Mar-2018

1-Aug-2018

63032EV00

1-Mar-2018

1-Aug-2018

63328EV00

1-Mar-2018

1-Aug-2018

63330EV00

1-Mar-2018

1-Aug-2018

63473EV00

1-Mar-2018

1-Aug-2018

63486EV00

1-Mar-2018

1-Aug-2018

64085EV00

1-Apr-2018

1-Sep-2018

64090EV00

1-Apr-2018

1-Sep-2018

65197EV00

1-May-2018

1-Oct-2018

65200EV00

1-May-2018

1-Oct-2018

65205EV00

1-May-2018

1-Oct-2018

65206EV00

1-May-2018

1-Oct-2018

65503EV00

1-May-2018

1-Oct-2018

65504EV00

1-May-2018

1-Oct-2018

67138EV00

1-Jul-2018

1-Dec-2018

67139EV00

1-Jul-2018

1-Dec-2018

67140EV00

1-Jul-2018

1-Dec-2018

67141EV00

1-Jul-2018

1-Dec-2018

67142EV00

1-Jul-2018

1-Dec-2018

67248EV00

1-Jul-2018

1-Dec-2018

67279EV00

1-Jul-2018

1-Dec-2018

67280EV00

1-Jul-2018

1-Dec-2018

67281EV00

1-Jul-2018

1-Dec-2018

67282EV00

1-Jul-2018

1-Dec-2018

67283EV00

1-Jul-2018

1-Dec-2018

67284EV00

1-Jul-2018

1-Dec-2018

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Sodium Bicarbonate Injection, USP 8.4% (1 mEq/mL); 50 mEq/50 mL Single Dose Glass Fliptop Vial (NDC 0409-6625-25) LABELLED AS NOVAPLUS

Product/
Lot Number

Manufacturer’s Original
Expiry Date

New Use Date
(beyond manufacturer’s original expiry date)

64083EV00

1-Apr-2018

1-Sep-2018

64084EV00

1-Apr-2018

1-Sep-2018

 

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Page Last Updated: 10/30/2018
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