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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 68071-4063 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA086727
Dosage form / routeTABLET · ORAL
Active ingredientsATROPINE SULFATE (.025 mg/1)
DIPHENOXYLATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20170620
Package count4

External sources

Source: openFDA. Public-domain (CC0).