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001OMNICEFCEFDINIRCAPSULE;ORAL300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo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 43.

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N050739-001OMNICEFCEFDINIR300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04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 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-0484e616aacf4f…
2026-08-18 06:07:402026-07N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-0431067a03dcf5…
2025-08-23 18:47 UTC2025-08N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-046a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-0403ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-042680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-045bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-0479d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-041e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-048072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-045c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050739-001OMNICEF300MGCAPSULE / ORALRLD1997-12-045d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050739-001OMNICEF300MGCAPSULE / ORALRLD1997-12-044b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-0474a2ff9319b5…
2022-03-09 01:35 UTC2022-03N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-04782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-0487673890dc5c…
2021-03-12 10:30 UTC2021-03N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-045aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-048869cabd3fbd…
2020-11-12 02:37 UTC2020-11N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-04c0c555d07b60…
2019-12-14 00:12 UTC2019-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-043f01610625f2…
2019-09-15 20:21 UTC2019-09N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-04b00525d2431f…
2019-07-19 19:46 UTC2019-07N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**CAPSULE / ORALRLD1997-12-04ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-046a51e52b5d6a…
2024-02-18 07:12 UTC2024-02N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-041c564ffb4f44…
2023-12-20 04:57 UTC2023-12N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-049b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-043f0d92c62455…
2023-05-13 08:27 UTC2023-05N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-04053a50430f4f…
2023-01-26 05:58 UTC2023-01N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-043bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11N050739-001OMNICEF300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE / ORALRLD1997-12-043a93d1ddd44b…
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…

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 3 of 4 · 70 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CEFDINIRCEFDINIRDIRECT RX982d0f53-20bc-1cb4-e053-2995a90ad33c2025-01-22WarningsName fallback
generic name: CEFDINIR
CEFDINIRCEFDINIRDirectRxd70b9e1f-908f-b570-e053-2995a90af0982025-01-21Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.c974d975-8616-3551-e053-2995a90a65f32025-01-14Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.54b06071-f3cb-5627-e054-00144ff8d46c2024-07-17Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.1bbd75ea-5a50-eb00-e063-6394a90a1cec2024-06-25WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.96cad498-70d3-3089-e053-2995a90a9d192024-06-19Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.8c3b89a9-cb3f-5960-e053-2995a90aaeee2024-06-18Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRNuCare Pharmaceuticals,Inc.8dfbad95-4dd8-01fd-e053-2a95a90a1de12024-06-18Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRAmerican Health Packagingc493e78b-afa3-4f74-8305-75e5f3817df02024-06-07Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutionsbeeb9480-f9f9-44ae-93f3-6f4da81888f52024-02-27Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRAurobindo Pharma Limited06fbdb63-d32f-4212-9962-f1de15597dda2024-02-14Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRRising Pharma Holdings, Inc.a5594006-8e37-459e-8e85-7e2a83d7a57e2024-02-12Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRAurobindo Pharma Limiteddf26edb0-9bd6-449c-a187-0be0c9e2600c2024-02-12Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutions10bf69e7-5f7e-4448-9f22-777f137d96662023-12-25Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
cefdinirCEFDINIRA-S Medication Solutions7bbcc4ac-c964-4c6b-88c0-11c0ba9933db2023-11-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutionsa217d454-4ca0-4b29-8a64-eb9393a852692023-11-21Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutions37b5d000-db9e-4b6e-8208-6361e98fb55d2023-11-01WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutions7c25ae35-61f4-4aef-a8d9-8de77b02ab802023-09-12Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LP506bcf51-3b7e-4fc0-b22e-a5b726471e3a2023-07-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRA-S Medication Solutionsfb02aaab-d2a0-466e-8327-72e3df1e4e9d2023-04-04Warnings, 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