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Tolterodine Tartrate

NDC 0093-0010 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077006
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOLTERODINE TARTRATE (1 mg/1)
Marketing started20151101
Package count1

External sources

Source: openFDA. Public-domain (CC0).