Ibuprofen

Product NDC
67296-1573
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
RedPharm Drug, Inc.
Application
ANDA202413
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67296-1573-330 TABLET in 1 BOTTLE (67296-1573-3) 2018-01-010000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ibuprofenRedPharm Drug, Inc.2020-01-20HUMAN PRESCRIPTION DRUG LABEL5