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Bethanechol Chloride

NDC 23155-935 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091256
Dosage form / routeTABLET · ORAL
Active ingredientsBETHANECHOL CHLORIDE (10 mg/1)
Marketing started20250630
Package count1

External sources

Source: openFDA. Public-domain (CC0).