FDA NDC Directory · JSON-LD · Markdown

Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 75826-107 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerWinder Laboratories LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211362
Dosage form / routeTABLET · ORAL
Active ingredientsATROPINE SULFATE (.025 mg/1)
DIPHENOXYLATE HYDROCHLORIDE (2.5 mg/1)
Marketing started20220430
Package count5

External sources

Source: openFDA. Public-domain (CC0).