Ibuprofen

Product NDC
68071-2947
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
68071-2947-121 TABLET in 1 BOTTLE (68071-2947-1) 2023-03-03NoHistorical
68071-2947-220 TABLET in 1 BOTTLE (68071-2947-2) 2023-03-03NoHistorical
68071-2947-330 TABLET in 1 BOTTLE (68071-2947-3) 2023-03-03NoHistorical
68071-2947-440 TABLET in 1 BOTTLE (68071-2947-4) 2025-10-30NoHistorical
68071-2947-550 TABLET in 1 BOTTLE (68071-2947-5) 2023-03-03NoHistorical
68071-2947-660 TABLET in 1 BOTTLE (68071-2947-6) 2023-03-03NoHistorical
68071-2947-990 TABLET in 1 BOTTLE (68071-2947-9) 2023-03-03NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyNuCare Pharmaceuticals,Inc.2025-10-30HUMAN PRESCRIPTION DRUG LABEL6
Ibuprofen Tablets, USP Rx onlyNuCare Pharmaceuticals,Inc.2023-06-06HUMAN PRESCRIPTION DRUG LABEL5