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

[February 27, 2019] This is to update and consolidate the information posted here previously on 6/15/17, 6/23/17, 7/19/17, 8/17/17,  11/9/2017, 6/12/2018, and 12/21/2018. 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 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)
  • 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)

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)
69292DK001-Sep-20181-Mar-2019
78264DK001-Jun-20191-Dec-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)
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
74033DK001-Feb-20191-Feb-2020
77115DK001-May-20191-May-2020
77194DK001-May-20191-May-2020
77237DK001-May-20191-May-2020
77238DK001-May-20191-May-2020
77320DK001-May-20191-May-2020

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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)
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
75406EV001-Mar-20191-Sep-2019
75407EV001-Mar-20191-Sep-2019
75408EV001-Mar-20191-Sep-2019
75409EV001-Mar-20191-Sep-2019
77031EV001-May-20191-Nov-2019
77033EV001-May-20191-Nov-2019
77034EV001-May-20191-Nov-2019
77068EV001-May-20191-Nov-2019
79022EV001-Jul-20191-Jan-2020
79023EV001-Jul-20191-Jan-2020

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Dextrose 50% Injection, USP (0.5 g/mL), 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)
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
77099DK001-May-20191-May-2020
77224DK001-May-20191-May-2020
77226DK001-May-20191-May-2020
77232DK001-May-20191-May-2020
77402DK001-May-20191-May-2020
78191DK001-Jun-20191-Jun-2020
78246DK001-Jun-20191-Jun-2020
78252DK001-Jun-20191-Jun-2020
79090DK001-Jul-20191-Jul-2020

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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)
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
77113DK001-Feb-20191-Nov-2019
77114DK001-Feb-20191-Nov-2019
77117DK001-Feb-20191-Nov-2019
77118DK001-Feb-20191-Nov-2019
77195DK001-Feb-20191-Nov-2019
77196DK001-Feb-20191-Nov-2019
77197DK001-Feb-20191-Nov-2019
77240DK001-Feb-20191-Nov-2019
77241DK001-Feb-20191-Nov-2019
77242DK001-Feb-20191-Nov-2019
77408DK001-Feb-20191-Nov-2019
78196DK001-Mar-20191-Dec-2019
78198DK001-Mar-20191-Dec-2019
78199DK001-Mar-20191-Dec-2019
78261DK001-Mar-20191-Dec-2019
78263DK001-Mar-20191-Dec-2019
78270DK001-Mar-20191-Dec-2019
78372DK001-Mar-20191-Dec-2019
80071DK001-May-20191-Feb-2020
80072DK001-May-20191-Feb-2020
80073DK001-May-20191-Feb-2020
80074DK001-May-20191-Feb-2020
80076DK001-May-20191-Feb-2020
80077DK001-May-20191-Feb-2020
80078DK001-May-20191-Feb-2020
80369DK001-May-20191-Feb-2020
81017DK001-Jun-20191-Mar-2020
81018DK001-Jun-20191-Mar-2020
81192DK001-Jun-20191-Mar-2020
81194DK001-Jun-20191-Mar-2020
81196DK001-Jun-20191-Mar-2020
81201DK001-Jun-20191-Mar-2020
81202DK001-Jun-20191-Mar-2020
81208DK001-Jun-20191-Mar-2020
81212DK001-Jun-20191-Mar-2020
81213DK001-Jun-20191-Mar-2020
81370DK001-Jun-20191-Mar-2020
81371DK001-Jun-20191-Mar-2020
82217DK001-Jul-20191-Apr-2020
82218DK001-Jul-20191-Apr-2020
82220DK001-Jul-20191-Apr-2020
82221DK001-Jul-20191-Apr-2020
82223DK001-Jul-20191-Apr-2020
82224DK001-Jul-20191-Apr-2020
82225DK001-Jul-20191-Apr-2020
82228DK001-Jul-20191-Apr-2020
82230DK001-Jul-20191-Apr-2020
82231DK001-Jul-20191-Apr-2020
82232DK001-Jul-20191-Apr-2020

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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)

69128DK001-Sep-20181-Mar-2019
69129DK001-Sep-20181-Mar-2019
69131DK001-Sep-20181-Mar-2019
69132DK001-Sep-20181-Mar-2019
69133DK001-Sep-20181-Mar-2019
69134DK001-Sep-20181-Mar-2019
69142DK001-Sep-20181-Mar-2019
69144DK001-Sep-20181-Mar-2019
69270DK001-Sep-20181-Mar-2019
69271DK001-Sep-20181-Mar-2019
69346DK001-Sep-20181-Mar-2019
69395DK001-Sep-20181-Mar-2019
69396DK001-Sep-20181-Mar-2019
69397DK001-Sep-20181-Mar-2019
70351DK001-Oct-20181-Apr-2019
73127DK001-Jan-20191-Jul-2019
73128DK001-Jan-20191-Jul-2019
73129DK001-Jan-20191-Jul-2019
73337DK001-Jan-20191-Jul-2019
74344DK001-Feb-20191-Aug-2019
76026DK001-Apr-20191-Oct-2019
76027DK001-Apr-20191-Oct-2019
76028DK001-Apr-20191-Oct-2019
76029DK001-Apr-20191-Oct-2019
76074DK001-Apr-20191-Oct-2019
76297DK001-Apr-20191-Oct-2019
76301DK001-Apr-20191-Oct-2019
76302DK001-Apr-20191-Oct-2019
76368DK001-Apr-20191-Oct-2019
77101DK001-May-20191-Nov-2019
77102DK001-May-20191-Nov-2019
77103DK001-May-20191-Nov-2019
77106DK001-May-20191-Nov-2019
77107DK001-May-20191-Nov-2019
77108DK001-May-20191-Nov-2019
77227DK001-May-20191-Nov-2019
77228DK001-May-20191-Nov-2019
77230DK001-May-20191-Nov-2019
77233DK001-May-20191-Nov-2019
77234DK001-May-20191-Nov-2019
77235DK001-May-20191-Nov-2019
78194DK001-Jun-20191-Dec-2019
78195DK001-Jun-20191-Dec-2019
78238DK001-Jun-20191-Dec-2019
78241DK001-Jun-20191-Dec-2019
78242DK001-Jun-20191-Dec-2019
78243DK001-Jun-20191-Dec-2019
78326DK001-Jun-20191-Dec-2019
78248DK001-Jun-20191-Dec-2019
78251DK001-Jun-20191-Dec-2019
79091DK001-Jul-20191-Jan-2020
79094DK001-Jul-20191-Jan-2020
79095DK001-Jul-20191-Jan-2020
79099DK001-Jul-20191-Jan-2020
79100DK001-Jul-20191-Jan-2020
79101DK001-Jul-20191-Jan-2020
79225DK001-Jul-20191-Jan-2020

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