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Ibuprofen

NDC 69842-489 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerCVS Pharmacy.Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091237
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20211218
Package count1

External sources

Source: openFDA. Public-domain (CC0).