FDA NDC Directory · JSON-LD · Markdown

MISOPROSTOL

NDC 42571-253 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMisoprostol
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216872
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (100 ug/1)
Marketing started20230101
Package count2

External sources

Source: openFDA. Public-domain (CC0).