FDA.reportPublic FDA data

Application 050739

Type
NDA
Sponsor
ABBVIE

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001OMNICEFCEFDINIRCAPSULE;ORAL300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N050739-001OMNICEFCEFDINIR300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 2 of 2 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2022-10-28 04:53 UTC2022-10N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04cb3db0bc1861…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04a50c72e98297…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 4 · 70 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CefdinirCEFDINIRNuCare Pharmaceuticals, Inc.5a72e445-b920-b97d-e063-6294a90af2ee2026-09-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRREMEDYREPACK INC.a8029f7c-6353-46db-8c8c-c86a9485a14f2026-08-28Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutions0eeac6df-bad7-413e-8b41-0660f3a993732026-08-20Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNorthwind Health Company, LLC1d0d50ba-8c2b-855c-e063-6394a90a5c7d2026-07-09Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LP63d2f931-6896-47e5-905e-4f812d6cb1052026-06-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals, Inc.5128dc70-f3cd-25c0-e063-6294a90aa52f2026-05-06Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals Inc.3714d558-cbaa-42e8-831b-ffbbc951ebf22026-04-21WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals Inc.5b6c1b5d-a1d5-4e08-9077-2af3f38fea4e2026-03-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals Inc.c3892cd7-0e98-4ba3-a845-4aedf6c2a8302026-03-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals Inc.2da6eb80-63b0-4377-8d7b-865733ebbab12026-03-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals Inc.0d1212c9-604f-4999-8f7d-e7cf300705ef2026-03-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
cefdinirCEFDINIRPreferred Pharmaceuticals Inc.2e384d98-642e-4841-9f62-fcea4c242f4e2026-03-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPreferred Pharmaceuticals, Inc.8787ea15-bf90-4178-9b0f-08b075f1aa3d2026-03-24WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.c23af6af-a97b-b98d-e053-2995a90ae7802026-03-13Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
cefdinirCEFDINIRA-S Medication Solutions2bd2101c-511d-45a9-b1d8-a45ed40c5b802026-03-12Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRPD-Rx Pharmaceuticals, Inc.a5f028d5-ab33-491e-a385-56e79e1651502026-02-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRREMEDYREPACK INC.eb354221-c476-41cb-ad87-52423f81d6982026-01-28Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRAvKARE1acc5d17-10a4-e23d-e063-6394a90a52c32026-01-13Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutions17b4e82f-4169-4ab9-bd4a-79781a71e1602025-12-19WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.9ba5cb2d-6272-27de-e053-2995a90a58c82025-12-03Warnings, Adverse reactionsName fallback
generic name: CEFDINIR

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
30415SUPPL2015-11-20
18147SUPPL2015-11-19
39220SUPPL2009-01-02
8149SUPPL2008-12-19
8148SUPPL2007-09-25
39219SUPPL2007-09-19
30414SUPPL2007-07-05
18146SUPPL2007-06-27
42709ORIG2006-01-03
30413SUPPL2005-07-21
18145SUPPL2005-07-21
30412SUPPL2004-09-03
8147SUPPL2002-07-24
39218SUPPL1999-11-24
30411SUPPL1999-11-24