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IBUPROFEN

NDC 62207-320 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules India Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202312
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20191114
Package count10

External sources

Source: openFDA. Public-domain (CC0).