Ibuprofen

Product NDC
67296-2184
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Redpharm Drug
Application
ANDA202413
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67296-2184-330 TABLET, FILM COATED in 1 BOTTLE (67296-2184-3) 20240523NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
44f5743f-8c98-dc4d-e063-6294a90a6dfaIbuprofen Tablets, USP 300 mg, 400 mg, 600 mg and 800 mgRedpharm Drug2025-12-02HUMAN PRESCRIPTION DRUG LABEL1