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Ibuprofen

NDC 63548-0185 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerPLD Acquisitions LLC DBA Avma Pharma Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA076460
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20130801
Package count0

External sources

Source: openFDA. Public-domain (CC0).