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Dicyclomine hydrochloride

NDC 0832-6052 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216760
Dosage form / routeTABLET · ORAL
Active ingredientsDICYCLOMINE HYDROCHLORIDE (20 mg/1)
Marketing started20221128
Marketing ended20260930
Package count2

External sources

Source: openFDA. Public-domain (CC0).