FDA NDC Directory · JSON-LD · Markdown

Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 62559-490 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerANI 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 started20170707
Package count2

External sources

Source: openFDA. Public-domain (CC0).