Ibuprofen

Product NDC
59726-139
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
P & L Development, LLC
Application
ANDA079129
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
59726-139-50500 TABLET, COATED in 1 BOTTLE, PLASTIC (59726-139-50) 2024-08-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsP & L Development, LLC2024-07-30HUMAN OTC DRUG LABEL3