Application 050749

Type
NDA
Sponsor
ABBVIE

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001OMNICEFCEFDINIRFOR SUSPENSION;ORAL125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
002OMNICEFCEFDINIRFOR SUSPENSION;ORAL250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo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 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N050749-001OMNICEFCEFDINIR125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04
N050749-002OMNICEFCEFDINIR250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29

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 3 · 86 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-0484e616aacf4f…
2026-09-14 22:38:342026-08N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-2984e616aacf4f…
2026-08-18 06:07:402026-07N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04caaa826d4ba7…
2026-08-18 06:07:402026-07N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04011fe1cb6892…
2026-02-19 14:30 UTC2026-02N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-0431067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-2931067a03dcf5…
2025-08-23 18:47 UTC2025-08N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-046a471c1ec25d…
2025-08-23 18:47 UTC2025-08N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-296a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-0403ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-2903ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-042680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-292680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-045bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-295bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04d8e5a09893c0…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04d06236e962d9…
2024-10-29 15:01 UTC2024-10N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-0479d66fd596c7…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-2979d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-04301d65b070ca…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-29301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-041e350fbaab3a…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-291e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-048072bd15b7f6…
2024-05-31 18:47 UTC2024-05N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-298072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD1997-12-045c6f7cd8ea54…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**FOR SUSPENSION / ORALRLD2004-07-295c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050749-001OMNICEF125MG/5MLFOR SUSPENSION / ORALRLD1997-12-045d02ea3f76ae…
2022-04-08 23:34 UTC2022-04N050749-002OMNICEF250MG/5MLFOR SUSPENSION / ORALRLD2004-07-295d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050749-001OMNICEF125MG/5MLFOR SUSPENSION / ORALRLD1997-12-044b0b4de00fa7…
2022-04-04 05:41 UTC2022-04N050749-002OMNICEF250MG/5MLFOR SUSPENSION / ORALRLD2004-07-294b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050749-001OMNICEF125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**FOR SUSPENSION / ORALRLD1997-12-0474a2ff9319b5…
2019-12-13 00:20 UTC2019-12N050749-002OMNICEF250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**FOR SUSPENSION / ORALRLD2004-07-2974a2ff9319b5…

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 4 of 4 · 70 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CefdinirCEFDINIRBluePoint Laboratoriese342b7cf-f527-476e-8119-b1fd81c58b552023-03-29Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRTeva Pharmaceuticals USA, Inc.a1f49fe1-b511-4f6b-a912-8ae8662d95a52023-02-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LPbe963e80-e298-49a0-a52f-3d4dcded7c8c2022-10-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LP8305b5d8-53b3-475a-b263-07d5fd81392a2022-09-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
cefdinirCEFDINIRAscend Laboratories, LLCefb5a975-75ec-46e1-ba84-f68d0b9bf36f2022-06-29Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LP444cd2c4-836d-40d5-a307-d719fe83e7632022-05-02WarningsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LPf22acd90-5dc4-406d-af78-5f9c3a6746472022-03-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRSandoz Inc38f6adf7-e26c-4764-8ec9-360813874dd42020-02-24Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRProficient Rx LPf30d01e3-0839-4928-a45a-b46c89aa454c2019-11-01Warnings, Adverse reactionsName fallback
generic name: CEFDINIR
CefdinirCEFDINIRTeva Pharmaceuticals USA, Inc.de3441e3-7fd2-4d29-a8b7-0f9b66e35c9c2018-08-31Warnings, 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
8173SUPPL2015-11-20
39243SUPPL2015-11-19
18169SUPPL2009-01-02
30438SUPPL2008-12-19
30437SUPPL2007-09-25
39242SUPPL2007-09-19
8172SUPPL2007-07-05
18168SUPPL2007-06-27
22216ORIG2006-01-03
39241SUPPL2005-07-21
8171SUPPL2005-07-21
30436SUPPL2004-09-03
8170SUPPL2004-07-30
30435SUPPL1999-07-14
18167SUPPL1999-07-14