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Misoprostol

NDC 82804-037 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA076095
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (200 ug/1)
Marketing started20220411
Package count5

External sources

Source: openFDA. Public-domain (CC0).