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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 69315-910 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namediphenoxylate hydrochloride and atropine sulfate
Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213413
Dosage form / routeTABLET · ORAL
Active ingredientsATROPINE SULFATE (.025 mg/1)
DIPHENOXYLATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20200315
Package count3

External sources

Source: openFDA. Public-domain (CC0).