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  1. Drug Safety and Availability

Extended Use Dates Provided by Pfizer

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 Number LOT # EXP. DATE NEW EXP. DATE
00409-4887-10 580074P 1-Oct-18 1-Oct-19
00409-4887-10 580084P 1-Oct-18 1-Oct-19
00409-4887-10 580094P 1-Oct-18 1-Oct-19
00409-4887-10 600104P 1-Dec-18 1-Dec-19
00409-4887-10 610104P 1-Jan-19 1-Jan-20
00409-4887-10 610124P 1-Jan-19 1-Jan-20
00409-4887-10 630034P 1-Feb-19 1-Feb-20
00409-4887-10 640064P 1-Feb-19 1-Feb-20
00409-4887-20 640174P 1-Feb-19 1-Feb-20
00409-4887-20 650214P 1-Feb-19 1-Feb-20
00409-4887-10 630044P 1-Mar-19 1-Mar-20
00409-4887-10 630064P 1-Mar-19 1-Mar-20
00409-4887-10 630104P 1-Mar-19 1-Mar-20
00409-4887-10 630154P 1-Mar-19 1-Mar-20
00409-4887-10 630144P 1-Mar-19 1-Mar-20
00409-4887-10 640014P 1-Mar-19 1-Mar-20
00409-4887-10 640054P 1-Mar-19 1-Mar-20
00409-4887-10 640074P 1-Mar-19 1-Mar-20
00409-4887-20 58427DK 10/1/2018 10/1/2019
00409-4887-50 58400DK 10/1/2018 10/1/2019
00409-4887-50 58401DK 10/1/2018 10/1/2019
00409-4887-50 58402DK 10/1/2018 10/1/2019
00409-4887-50 58403DK 10/1/2018 10/1/2019
00409-4887-50 58408DK 10/1/2018 10/1/2019
00409-4887-10 58157DK 10/1/2018 10/1/2019
00409-4887-10 58158DK 10/1/2018 10/1/2019
00409-4887-10 58159DK 10/1/2018 10/1/2019
00409-4887-10 58160DK 10/1/2018 10/1/2019
00409-4887-10 58246DK 10/1/2018 10/1/2019
00409-4887-10 58247DK 10/1/2018 10/1/2019
00409-4887-10 58250DK 10/1/2018 10/1/2019
00409-4887-10 58442DK 10/1/2018 10/1/2019
00409-4887-20 59002DK 11/1/2018 11/1/2019
00409-4887-20 59003DK 11/1/2018 11/1/2019
00409-4887-20 59102DK 11/1/2018 11/1/2019
00409-4887-20 59419DK 11/1/2018 11/1/2019
00409-4887-20 59420DK 11/1/2018 11/1/2019
00409-4887-10 59012DK 11/1/2018 11/1/2019
00409-4887-10 59013DK 11/1/2018 11/1/2019
00409-4887-10 59319DK 11/1/2018 11/1/2019
00409-4887-10 59349DK 11/1/2018 11/1/2019
00409-4887-10 59350DK 11/1/2018 11/1/2019
00409-4887-10 59351DK 11/1/2018 11/1/2019
00409-4887-10 59378DK 11/1/2018 11/1/2019
00409-4887-10 59379DK 11/1/2018 11/1/2019
00409-4887-10 59380DK 11/1/2018 11/1/2019
00409-4887-10 59381DK 11/1/2018 11/1/2019
00409-4887-20 60054DK 12/1/2018 12/1/2019
00409-4887-20 60055DK 12/1/2018 12/1/2019
00409-4887-20 60056DK 12/1/2018 12/1/2019
00409-4887-10 60015DK 12/1/2018 12/1/2019
00409-4887-10 60016DK 12/1/2018 12/1/2019
00409-4887-20 61005DK 1/1/2019 1/1/2020
00409-4887-20 61006DK 1/1/2019 1/1/2020
00409-4887-20 61007DK 1/1/2019 1/1/2020
00409-4887-20 61008DK 1/1/2019 1/1/2020
00409-4887-20 61010DK 1/1/2019 1/1/2020
00409-4887-20 61299DK 1/1/2019 1/1/2020
00409-4887-20 61366DK 1/1/2019 1/1/2020
00409-4887-20 61368DK 1/1/2019 1/1/2020
00409-4887-50 61099DK 1/1/2019 1/1/2020
00409-4887-50 61363DK 1/1/2019 1/1/2020
00409-4887-99 61276DK 1/1/2019 1/1/2020
00409-4887-99 61279DK 1/1/2019 1/1/2020
00409-4887-99 61280DK 1/1/2019 1/1/2020
00409-4887-10 61062DK 1/1/2019 1/1/2020
00409-4887-10 61063DK 1/1/2019 1/1/2020
00409-4887-10 61064DK 1/1/2019 1/1/2020
00409-4887-20 62018DK 2/1/2019 2/2/2020
00409-4887-20 62019DK 2/1/2019 2/2/2020
00409-4887-20 62418DK 2/1/2019 2/2/2020
00409-4887-50 62290DK 2/1/2019 2/2/2020
00409-4887-99 62316DK 2/1/2019 2/2/2020
00409-4887-99 62317DK 2/1/2019 2/2/2020
00409-4887-99 62318DK 2/1/2019 2/2/2020
00409-4887-99 62319DK 2/1/2019 2/2/2020
00409-4887-10 62228DK 2/1/2019 2/2/2020
00409-4887-10 62229DK 2/1/2019 2/2/2020
00409-4887-10 62230DK 2/1/2019 2/2/2020
00409-4887-20 63443DK 3/1/2019 3/1/2020
00409-4887-20 63444DK 3/1/2019 3/1/2020
00409-4887-20 63445DK 3/1/2019 3/1/2020
00409-4887-20 63446DK 3/1/2019 3/1/2020
00409-4887-50 63278DK 3/1/2019 3/1/2020
00409-4887-50 63279DK 3/1/2019 3/1/2020
00409-4887-50 63280DK 3/1/2019 3/1/2020
00409-4887-50 63462DK 3/1/2019 3/1/2020
00409-4887-50 63463DK 3/1/2019 3/1/2020
00409-4887-99 63170DK 3/1/2019 3/1/2020
00409-4887-99 63425DK 3/1/2019 3/1/2020
00409-4887-99 63426DK 3/1/2019 3/1/2020

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 NUMBER LOT # MFG. DATE EXP DATE NEW EXP DATE
00409-5921-01 76328DK 4/12/2017 10/1/2018 2/1/2019
00409-5921-01 76329DK 4/13/2017 10/1/2018 2/1/2019
00409-5921-01 76330DK 4/17/2017 10/1/2018 2/1/2019
00409-5922-01 76331DK 4/18/2017 10/1/2018 2/1/2019

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

Batch Manufacturer's Original
Expiration Date
New Expiration Date
(beyond manufacturer's
original expiry date)
6FM722 4/2018 8/2018
6FM739 4/2018 8/2018
6FM771 4/2018 8/2018
6FM772 4/2018 8/2018
6FM773 4/2018 8/2018
6FM715 5/2018 9/2018
6FM716 5/2018 9/2018
6FM756 5/2018 9/2018
6FM757 5/2018 9/2018
6FM768 5/2018 9/2018
6FM780 5/2018 9/2018
6FM781 5/2018 9/2018
6FM782 5/2018 9/2018
6FM783 5/2018 9/2018
6FM785 6/2018 10/2018
6FM787 6/2018 10/2018
7FM115 8/2018 12/2018
7FM117 8/2018 12/2018
7FM120 8/2018 12/2018
7FM134 8/2018 12/2018
7FM174 9/2018 1/2019
7FM175 9/2018 1/2019
7FM274 10/2018 2/2019
7FM275 10/2018 2/2019
7FM276 10/2018 2/2019

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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
 

Batch Manufacturer's Original
Expiration Date
New Expiration Date
(beyond manufacturer's
original expiry date)
6GM480 4/2018 8/2018
6GM481 4/2018 8/2018
6GM503 4/2018 8/2018
6GM504 4/2018 8/2018
6GM506 4/2018 8/2018
6GM507 4/2018 8/2018
6GM512 4/2018 8/2018
6GM669 4/2018 8/2018
6GM599 5/2018 9/2018
6GM685 6/2018 10/2018
6GM766 6/2018 10/2018
6GM767 6/2018 10/2018
7GM026 8/2018 12/2018
7GM045 8/2018 12/2018
7GM048 9/2018 1/2019
7GM054 9/2018 1/2019
7GM164 9/2018 1/2019
7GM172 9/2018 1/2019
7GM173 9/2018 1/2019
7GM272 9/2018 1/2019
7GM191 10/2018 2/2019
7GM200 11/2018 3/2019
7GM201 11/2018 3/2019
7GM203 12/2018 4/2019
7GM204 12/2018 4/2019
7GM212 12/2018 4/2019
7GM213 12/2018 4/2019
7GM360 12/2018 4/2019
7GM361 12/2018 4/2019

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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)
69292DK00 1-Sep-2018 1-Mar-2019
78264DK00 1-Jun-2019 1-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)
63292DK00 1-Mar-2018 1-Mar-2019
63293DK00 1-Mar-2018 1-Mar-2019
63318DK00 1-Mar-2018 1-Mar-2019
63319DK00 1-Mar-2018 1-Mar-2019
64271DK00 1-Apr-2018 1-Apr-2019
64301DK00 1-Apr-2018 1-Apr-2019
64302DK00 1-Apr-2018 1-Apr-2019
65255DK00 1-May-2018 1-May-2019
66267DK00 1-Jun-2018 1-Jun-2019
67259DK00 1-Jul-2018 1-Jul-2019
67302DK00 1-Jul-2018 1-Jul-2019
71343DK00  1-Nov-2018  1-Nov-2019
74033DK00 1-Feb-2019 1-Feb-2020
77115DK00 1-May-2019 1-May-2020
77194DK00 1-May-2019 1-May-2020
77237DK00 1-May-2019 1-May-2020
77238DK00 1-May-2019 1-May-2020
77320DK00 1-May-2019 1-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)
70046EV00 1-Oct-2018 1-Apr-2019
70047EV00 1-Oct-2018 1-Apr-2019
70048EV00 1-Oct-2018 1-Apr-2019
70049EV00 1-Oct-2018 1-Apr-2019
71130EV00 1-Nov-2018 1-May-2019
71197EV00 1-Nov-2018 1-May-2019
71319EV00 1-Nov-2018 1-May-2019
75406EV00 1-Mar-2019 1-Sep-2019
75407EV00 1-Mar-2019 1-Sep-2019
75408EV00 1-Mar-2019 1-Sep-2019
75409EV00 1-Mar-2019 1-Sep-2019
77031EV00 1-May-2019 1-Nov-2019
77033EV00 1-May-2019 1-Nov-2019
77034EV00 1-May-2019 1-Nov-2019
77068EV00 1-May-2019 1-Nov-2019
79022EV00 1-Jul-2019 1-Jan-2020
79023EV00 1-Jul-2019 1-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)
63391DK00 1-Mar-2018 1-Mar-2019
63392DK00 1-Mar-2018 1-Mar-2019
63475DK00 1-Mar-2018 1-Mar-2019
64278DK00 1-Apr-2018 1-Apr-2019
64282DK00 1-Apr-2018 1-Apr-2019
65468DK00 1-May-2018 1-May-2019
66007DK00 1-Jun-2018 1-Jun-2019
66387DK00 1-Jun-2018 1-Jun-2019
67040DK00 1-Jul-2018 1-Jul-2019
67041DK00 1-Jul-2018 1-Jul-2019
67042DK00 1-Jul-2018 1-Jul-2019
68082DK00 1-Aug-2018  1-Aug-2019
68458DK00 1-Aug-2018  1-Aug-2019
77099DK00 1-May-2019 1-May-2020
77224DK00 1-May-2019 1-May-2020
77226DK00 1-May-2019 1-May-2020
77232DK00 1-May-2019 1-May-2020
77402DK00 1-May-2019 1-May-2020
78191DK00 1-Jun-2019 1-Jun-2020
78246DK00 1-Jun-2019 1-Jun-2020
78252DK00 1-Jun-2019 1-Jun-2020
79090DK00 1-Jul-2019 1-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)
69171DK00 1-Jun-2018 1-Mar-2019
69172DK00 1-Jun-2018 1-Mar-2019
69273DK00 1-Jun-2018 1-Mar-2019
69274DK00 1-Jun-2018 1-Mar-2019
69278DK00 1-Jun-2018 1-Mar-2019
70265DK00 1-Jul-2018 1-Apr-2019
76158DK00 1-Jan-2019 1-Oct-2019
76159DK00 1-Jan-2019 1-Oct-2019
77113DK00 1-Feb-2019 1-Nov-2019
77114DK00 1-Feb-2019 1-Nov-2019
77117DK00 1-Feb-2019 1-Nov-2019
77118DK00 1-Feb-2019 1-Nov-2019
77195DK00 1-Feb-2019 1-Nov-2019
77196DK00 1-Feb-2019 1-Nov-2019
77197DK00 1-Feb-2019 1-Nov-2019
77240DK00 1-Feb-2019 1-Nov-2019
77241DK00 1-Feb-2019 1-Nov-2019
77242DK00 1-Feb-2019 1-Nov-2019
77408DK00 1-Feb-2019 1-Nov-2019
78196DK00 1-Mar-2019 1-Dec-2019
78198DK00 1-Mar-2019 1-Dec-2019
78199DK00 1-Mar-2019 1-Dec-2019
78261DK00 1-Mar-2019 1-Dec-2019
78263DK00 1-Mar-2019 1-Dec-2019
78270DK00 1-Mar-2019 1-Dec-2019
78372DK00 1-Mar-2019 1-Dec-2019
80071DK00 1-May-2019 1-Feb-2020
80072DK00 1-May-2019 1-Feb-2020
80073DK00 1-May-2019 1-Feb-2020
80074DK00 1-May-2019 1-Feb-2020
80076DK00 1-May-2019 1-Feb-2020
80077DK00 1-May-2019 1-Feb-2020
80078DK00 1-May-2019 1-Feb-2020
80369DK00 1-May-2019 1-Feb-2020
81017DK00 1-Jun-2019 1-Mar-2020
81018DK00 1-Jun-2019 1-Mar-2020
81192DK00 1-Jun-2019 1-Mar-2020
81194DK00 1-Jun-2019 1-Mar-2020
81196DK00 1-Jun-2019 1-Mar-2020
81201DK00 1-Jun-2019 1-Mar-2020
81202DK00 1-Jun-2019 1-Mar-2020
81208DK00 1-Jun-2019 1-Mar-2020
81212DK00 1-Jun-2019 1-Mar-2020
81213DK00 1-Jun-2019 1-Mar-2020
81370DK00 1-Jun-2019 1-Mar-2020
81371DK00 1-Jun-2019 1-Mar-2020
82217DK00 1-Jul-2019 1-Apr-2020
82218DK00 1-Jul-2019 1-Apr-2020
82220DK00 1-Jul-2019 1-Apr-2020
82221DK00 1-Jul-2019 1-Apr-2020
82223DK00 1-Jul-2019 1-Apr-2020
82224DK00 1-Jul-2019 1-Apr-2020
82225DK00 1-Jul-2019 1-Apr-2020
82228DK00 1-Jul-2019 1-Apr-2020
82230DK00 1-Jul-2019 1-Apr-2020
82231DK00 1-Jul-2019 1-Apr-2020
82232DK00 1-Jul-2019 1-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)

69128DK00 1-Sep-2018 1-Mar-2019
69129DK00 1-Sep-2018 1-Mar-2019
69131DK00 1-Sep-2018 1-Mar-2019
69132DK00 1-Sep-2018 1-Mar-2019
69133DK00 1-Sep-2018 1-Mar-2019
69134DK00 1-Sep-2018 1-Mar-2019
69142DK00 1-Sep-2018 1-Mar-2019
69144DK00 1-Sep-2018 1-Mar-2019
69270DK00 1-Sep-2018 1-Mar-2019
69271DK00 1-Sep-2018 1-Mar-2019
69346DK00 1-Sep-2018 1-Mar-2019
69395DK00 1-Sep-2018 1-Mar-2019
69396DK00 1-Sep-2018 1-Mar-2019
69397DK00 1-Sep-2018 1-Mar-2019
70351DK00 1-Oct-2018 1-Apr-2019
73127DK00 1-Jan-2019 1-Jul-2019
73128DK00 1-Jan-2019 1-Jul-2019
73129DK00 1-Jan-2019 1-Jul-2019
73337DK00 1-Jan-2019 1-Jul-2019
74344DK00 1-Feb-2019 1-Aug-2019
76026DK00 1-Apr-2019 1-Oct-2019
76027DK00 1-Apr-2019 1-Oct-2019
76028DK00 1-Apr-2019 1-Oct-2019
76029DK00 1-Apr-2019 1-Oct-2019
76074DK00 1-Apr-2019 1-Oct-2019
76297DK00 1-Apr-2019 1-Oct-2019
76301DK00 1-Apr-2019 1-Oct-2019
76302DK00 1-Apr-2019 1-Oct-2019
76368DK00 1-Apr-2019 1-Oct-2019
77101DK00 1-May-2019 1-Nov-2019
77102DK00 1-May-2019 1-Nov-2019
77103DK00 1-May-2019 1-Nov-2019
77106DK00 1-May-2019 1-Nov-2019
77107DK00 1-May-2019 1-Nov-2019
77108DK00 1-May-2019 1-Nov-2019
77227DK00 1-May-2019 1-Nov-2019
77228DK00 1-May-2019 1-Nov-2019
77230DK00 1-May-2019 1-Nov-2019
77233DK00 1-May-2019 1-Nov-2019
77234DK00 1-May-2019 1-Nov-2019
77235DK00 1-May-2019 1-Nov-2019
78194DK00 1-Jun-2019 1-Dec-2019
78195DK00 1-Jun-2019 1-Dec-2019
78238DK00 1-Jun-2019 1-Dec-2019
78241DK00 1-Jun-2019 1-Dec-2019
78242DK00 1-Jun-2019 1-Dec-2019
78243DK00 1-Jun-2019 1-Dec-2019
78326DK00 1-Jun-2019 1-Dec-2019
78248DK00 1-Jun-2019 1-Dec-2019
78251DK00 1-Jun-2019 1-Dec-2019
79091DK00 1-Jul-2019 1-Jan-2020
79094DK00 1-Jul-2019 1-Jan-2020
79095DK00 1-Jul-2019 1-Jan-2020
79099DK00 1-Jul-2019 1-Jan-2020
79100DK00 1-Jul-2019 1-Jan-2020
79101DK00 1-Jul-2019 1-Jan-2020
79225DK00 1-Jul-2019 1-Jan-2020

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