FDA NDC Directory · JSON-LD · Markdown

Misoprostol

NDC 72789-300 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076095
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (200 ug/1)
Marketing started20220411
Package count3

External sources

Source: openFDA. Public-domain (CC0).