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Dicyclomine Hydrochloride

NDC 67296-2226 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217916
Dosage form / routeTABLET · ORAL
Active ingredientsDICYCLOMINE HYDROCHLORIDE (20 mg/1)
Marketing started20230913
Package count1

External sources

Source: openFDA. Public-domain (CC0).