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Ibuprofen

NDC 63868-979 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerCHAIN DRUG MARKETING ASSOCIATION INC
Marketing categoryAbbreviated NDA (generic) · App ANDA075010
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19880524
Marketing ended20280228
Package count3

External sources

Source: openFDA. Public-domain (CC0).