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Mesalamine

NDC 0480-7750 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213191
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsMESALAMINE (800 mg/1)
Marketing started20240822
Package count1

External sources

Source: openFDA. Public-domain (CC0).