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Dicyclomine Hydrochloride

NDC 68071-3555 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040317
Dosage form / routeTABLET · ORAL
Active ingredientsDICYCLOMINE HYDROCHLORIDE (20 mg/1)
Marketing started20230425
Package count2

External sources

Source: openFDA. Public-domain (CC0).