FDA NDC Directory · JSON-LD · Markdown

Misoprostol

NDC 68071-3762 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076095
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (100 ug/1)
Marketing started20220411
Package count2

External sources

Source: openFDA. Public-domain (CC0).