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Ibuprofen

NDC 59726-046 · HUMAN OTC DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerP & L Development, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207753
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20201204
Marketing ended20270201
Package count3

External sources

Source: openFDA. Public-domain (CC0).