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Bethanechol Chloride

NDC 65162-571 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040855
Dosage form / routeTABLET · ORAL
Active ingredientsBETHANECHOL CHLORIDE (5 mg/1)
Marketing started20071121
Package count3

External sources

Source: openFDA. Public-domain (CC0).