Ibuprofen

Product NDC
68071-2998
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA213794
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-2998-66 TABLET in 1 BOTTLE (68071-2998-6) 2023-05-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyNuCare Pharmaceuticals,Inc.2025-02-04HUMAN PRESCRIPTION DRUG LABEL2
Ibuprofen Tablets, USP Rx onlyNuCare Pharmaceuticals,Inc.2023-05-04HUMAN PRESCRIPTION DRUG LABEL1