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Misoprostol

NDC 43386-161 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLupin Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091667
Dosage form / routeTABLET · ORAL
Active ingredientsMISOPROSTOL (200 ug/1)
Marketing started20120725
Package count2

External sources

Source: openFDA. Public-domain (CC0).