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Trospium Chloride

NDC 70518-4593 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204945
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTROSPIUM CHLORIDE (20 mg/1)
Marketing started20260323
Package count4

External sources

Source: openFDA. Public-domain (CC0).