FDA NDC Directory · JSON-LD · Markdown

Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 60687-890 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namediphenoxylate hydrochloride and atropine sulfate
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA213335
Dosage form / routeTABLET · ORAL
Active ingredientsATROPINE SULFATE (.025 mg/1)
DIPHENOXYLATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20250801
Package count1

External sources

Source: openFDA. Public-domain (CC0).