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Ibuprofen 200mg

NDC 69822-693 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerSouthern Sales & Services, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20221031
Package count1

External sources

Source: openFDA. Public-domain (CC0).