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Ibuprofen

NDC 50844-438 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameibuprofen
Labeler / ManufacturerL.N.K. International, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075139
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19990301
Package count3

External sources

Source: openFDA. Public-domain (CC0).