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Misoprostol

NDC 54348-148 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMISOPROSTOL
Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091667
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (200 ug/1)
Marketing started20190710
Package count8

External sources

Source: openFDA. Public-domain (CC0).