FDA NDC Directory · JSON-LD · Markdown

TROSPIUM CHLORIDE

NDC 62135-742 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204945
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTROSPIUM CHLORIDE (20 mg/1)
Marketing started20160830
Package count1

External sources

Source: openFDA. Public-domain (CC0).