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Dicyclomine hydrochloride

NDC 60760-802 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerST. MARY'S MEDICAL PARK PHARMACY
Marketing categoryAbbreviated NDA (generic) · App ANDA216736
Dosage form / routeTABLET · ORAL
Active ingredientsDICYCLOMINE HYDROCHLORIDE (20 mg/1)
Marketing started20221214
Package count1

External sources

Source: openFDA. Public-domain (CC0).