FDA NDC Directory · JSON-LD · Markdown

Tolterodine Tartrate

NDC 29300-239 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205399
Dosage form / routeTABLET · ORAL
Active ingredientsTOLTERODINE TARTRATE (1 mg/1)
Marketing started20200805
Package count2

External sources

Source: openFDA. Public-domain (CC0).