Drugs

Extended Use Dates Provided by Pfizer

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 76328DK00 4/12/2017 10/1/2018 2/1/2019
00409-5921-01 76329DK00 4/13/2017 10/1/2018 2/1/2019
00409-5921-01 76330DK00 4/17/2017 10/1/2018 2/1/2019
00409-5922-01 76331DK00 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

[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)
63183DK00 1-Mar-2018 1-Sep-2018
64293DK00 1-Apr-2018 1-Oct-2018
67331DK00 1-Jul-2018 1-Jan-2019
69292DK00 1-Sep-2018 1-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)
56053DK00 1-Aug-2017 1-Aug-2018
57032DK00 1-Sep-2017 1-Sep-2018
57033DK00 1-Sep-2017 1-Sep-2018
57034DK00 1-Sep-2017 1-Sep-2018
57035DK00 1-Sep-2017 1-Sep-2018
58004DK00 1-Oct-2017 1-Oct-2018
58006DK00 1-Oct-2017 1-Oct-2018
58007DK00 1-Oct-2017 1-Oct-2018
58424DK00 1-Oct-2017 1-Oct-2018
58425DK00 1-Oct-2017 1-Oct-2018
59039DK00 1-Nov-2017 1-Nov-2018
59051DK00 1-Nov-2017 1-Nov-2018
59052DK00 1-Nov-2017 1-Nov-2018
59384DK00 1-Nov-2017 1-Nov-2018
62470DK00 1-Feb-2018 1-Feb-2019
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

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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)
62292EV00 1-Feb-2018 1-Aug-2018
62294EV00 1-Feb-2018 1-Aug-2018
68327EV00 1-Aug-2018 1-Feb-2019
68328EV00 1-Aug-2018 1-Feb-2019
68439EV00 1-Aug-2018 1-Feb-2019
68440EV00 1-Aug-2018 1-Feb-2019
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

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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)
55177DK00 1-Jul-2017 1-Jul-2018
55178DK00 1-Jul-2017 1-Jul-2018
56025DK00 1-Aug-2017 1-Aug-2018
56160DK00 1-Aug-2017 1-Aug-2018
56162DK00 1-Aug-2017 1-Aug-2018
58131DK00 1-Oct-2017 1-Oct-2018
59027DK00 1-Nov-2017 1-Nov-2018
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

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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)
61036EV00 1-Jan-2018 1-Jul-2018
61037EV00 1-Jan-2018 1-Jul-2018
61038EV00 1-Jan-2018 1-Jul-2018
61103EV00 1-Jan-2018 1-Jul-2018
61201EV00 1-Jan-2018 1-Jul-2018
61318EV00 1-Jan-2018 1-Jul-2018
61319EV00 1-Jan-2018 1-Jul-2018
61320EV00 1-Jan-2018 1-Jul-2018
62094EV00 1-Feb-2018 1-Aug-2018
62095EV00 1-Feb-2018 1-Aug-2018
62096EV00 1-Feb-2018 1-Aug-2018
62097EV00 1-Feb-2018 1-Aug-2018
63023EV00 1-Mar-2018 1-Sep-2018
63024EV00 1-Mar-2018 1-Sep-2018
63025EV00 1-Mar-2018 1-Sep-2018
63119EV00 1-Mar-2018 1-Sep-2018
63490EV00 1-Mar-2018 1-Sep-2018
63491EV00 1-Mar-2018 1-Sep-2018
63492EV00 1-Mar-2018 1-Sep-2018
63493EV00 1-Mar-2018 1-Sep-2018
64333EV00 1-Apr-2018 1-Oct-2018
64334EV00 1-Apr-2018 1-Oct-2018
64335EV00 1-Apr-2018 1-Oct-2018
65411EV00 1-May-2018 1-Nov-2018
65413EV00 1-May-2018 1-Nov-2018
65482EV00 1-May-2018 1-Nov-2018
65483EV00 1-May-2018 1-Nov-2018
66203EV00 1-Jun-2018 1-Dec-2018
66204EV00 1-Jun-2018 1-Dec-2018
66205EV00 1-Jun-2018 1-Dec-2018
67171EV00 1-Jul-2018 1-Jan-2019
67329EV00 1-Jul-2018 1-Jan-2019
68009EV00 1-Aug-2018 1-Feb-2019
68010EV00 1-Aug-2018 1-Feb-2019
68011EV00 1-Aug-2018 1-Feb-2019
68187EV00 1-Aug-2018 1-Feb-2019
68188EV00 1-Aug-2018 1-Feb-2019
68189EV00 1-Aug-2018 1-Feb-2019
68190EV00 1-Aug-2018 1-Feb-2019
69098EV00 1-Sep-2018 1-Mar-2019
69099EV00 1-Sep-2018 1-Mar-2019
69100EV00 1-Sep-2018 1-Mar-2019
69101EV00 1-Sep-2018 1-Mar-2019
69102EV00 1-Sep-2018 1-Mar-2019
69188EV00 1-Sep-2018 1-Mar-2019
69189EV00 1-Sep-2018 1-Mar-2019
69190EV00 1-Sep-2018 1-Mar-2019
69191EV00 1-Sep-2018 1-Mar-2019
69192EV00 1-Sep-2018 1-Mar-2019
70189EV00 1-Oct-2018 1-Apr-2019
70190EV00 1-Oct-2018 1-Apr-2019
70191EV00 1-Oct-2018 1-Apr-2019
70192EV00 1-Oct-2018 1-Apr-2019
71190EV00 1-Nov-2018 1-May-2019
71191EV00 1-Nov-2018 1-May-2019
71192EV00 1-Nov-2018 1-May-2019
71193EV00 1-Nov-2018 1-May-2019
71323EV00 1-Nov-2018 1-May-2019
71324EV00 1-Nov-2018 1-May-2019
71325EV00 1-Nov-2018 1-May-2019
71326EV00 1-Nov-2018 1-May-2019
72102EV00 1-Dec-2018 1-Jun-2019
72103EV00 1-Dec-2018 1-Jun-2019
72104EV00 1-Dec-2018 1-Jun-2019
72105EV00 1-Dec-2018 1-Jun-2019
73059EV00 1-Jan-2019 1-Jul-2019
73060EV00 1-Jan-2019 1-Jul-2019
73061EV00 1-Jan-2019 1-Jul-2019
73062EV00 1-Jan-2019 1-Jul-2019
73140EV00 1-Jan-2019 1-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)
62359DK00 1-Nov-2017 1-Aug-2018
62360DK00 1-Nov-2017 1-Aug-2018
62404DK00 1-Nov-2017 1-Aug-2018
62405DK00 1-Nov-2017 1-Aug-2018
62406DK00 1-Nov-2017 1-Aug-2018
62407DK00 1-Nov-2017 1-Aug-2018
62409DK00 1-Nov-2017 1-Aug-2018
62414DK00 1-Nov-2017 1-Aug-2018
62415DK00 1-Nov-2017 1-Aug-2018
62416DK00 1-Nov-2017 1-Aug-2018
62417DK00 1-Nov-2017 1-Aug-2018
62447DK00 1-Nov-2017 1-Aug-2018
62485DK00 1-Nov-2017 1-Aug-2018
63161DK00 1-Dec-2017 1-Sep-2018
63162DK00 1-Dec-2017 1-Sep-2018
63163DK00 1-Dec-2017 1-Sep-2018
63164DK00 1-Dec-2017 1-Sep-2018
63173DK00 1-Dec-2017 1-Sep-2018
63175DK00 1-Dec-2017 1-Sep-2018
63180DK00 1-Dec-2017 1-Sep-2018
63263DK00 1-Dec-2017 1-Sep-2018
63264DK00 1-Dec-2017 1-Sep-2018
63265DK00 1-Dec-2017 1-Sep-2018
63266DK00 1-Dec-2017 1-Sep-2018
63267DK00 1-Dec-2017 1-Sep-2018
63294DK00 1-Dec-2017 1-Sep-2018
63295DK00 1-Dec-2017 1-Sep-2018
63296DK00 1-Dec-2017 1-Sep-2018
63297DK00 1-Dec-2017 1-Sep-2018
63393DK00 1-Dec-2017 1-Sep-2018
64268DK00 1-Jan-2018 1-Oct-2018
64269DK00 1-Jan-2018 1-Oct-2018
64270DK00 1-Jan-2018 1-Oct-2018
64294DK00 1-Jan-2018 1-Oct-2018
64295DK00 1-Jan-2018 1-Oct-2018
64296DK00 1-Jan-2018 1-Oct-2018
64303DK00 1-Jan-2018 1-Oct-2018
64304DK00 1-Jan-2018 1-Oct-2018
64305DK00 1-Jan-2018 1-Oct-2018
64307DK00 1-Jan-2018 1-Oct-2018
64308DK00 1-Jan-2018 1-Oct-2018
64309DK00 1-Jan-2018 1-Oct-2018
65054DK00 1-Feb-2018 1-Nov-2018
65068DK00 1-Feb-2018 1-Nov-2018
65069DK00 1-Feb-2018 1-Nov-2018
65070DK00 1-Feb-2018 1-Nov-2018
65244DK00 1-Feb-2018 1-Nov-2018
65245DK00 1-Feb-2018 1-Nov-2018
65246DK00 1-Feb-2018 1-Nov-2018
65248DK00 1-Feb-2018 1-Nov-2018
65249DK00 1-Feb-2018 1-Nov-2018
65250DK00 1-Feb-2018 1-Nov-2018
65251DK00 1-Feb-2018 1-Nov-2018
65252DK00 1-Feb-2018 1-Nov-2018
66010DK00 1-Mar-2018 1-Dec-2018
66011DK00 1-Mar-2018 1-Dec-2018
66056DK00 1-Mar-2018 1-Dec-2018
66130DK00 1-Mar-2018 1-Dec-2018
66155DK00 1-Mar-2018 1-Dec-2018
66157DK00 1-Mar-2018 1-Dec-2018
66161DK00 1-Mar-2018 1-Dec-2018
66162DK00 1-Mar-2018 1-Dec-2018
66250DK00 1-Mar-2018 1-Dec-2018
66253DK00 1-Mar-2018 1-Dec-2018
66264DK00 1-Mar-2018 1-Dec-2018
67016DK00 1-Apr-2018 1-Jan-2019
67075DK00 1-Apr-2018 1-Jan-2019
67076DK00 1-Apr-2018 1-Jan-2019
67078DK00 1-Apr-2018 1-Jan-2019
67079DK00 1-Apr-2018 1-Jan-2019
67080DK00 1-Apr-2018 1-Jan-2019
67081DK00 1-Apr-2018 1-Jan-2019
67085DK00 1-Apr-2018 1-Jan-2019
67086DK00 1-Apr-2018 1-Jan-2019
67087DK00 1-Apr-2018 1-Jan-2019
67088DK00 1-Apr-2018 1-Jan-2019
68086DK00 1-May-2018 1-Feb-2019
68087DK00 1-May-2018 1-Feb-2019
68090DK00 1-May-2018 1-Feb-2019
68091DK00 1-May-2018 1-Feb-2019
68092DK00 1-May-2018 1-Feb-2019
68094DK00 1-May-2018 1-Feb-2019
68096DK00 1-May-2018 1-Feb-2019
68097DK00 1-May-2018 1-Feb-2019
68098DK00 1-May-2018 1-Feb-2019
68155DK00 1-May-2018 1-Feb-2019
68156DK00 1-May-2018 1-Feb-2019
68316DK00 1-May-2018 1-Feb-2019
68317DK00 1-May-2018 1-Feb-2019
68398DK00 1-May-2018 1-Feb-2019
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

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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: 09/14/2018
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