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Tolterodine Tartrate

NDC 43975-322 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204562
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsTOLTERODINE TARTRATE (2 mg/1)
Marketing started20190829
Package count3

External sources

Source: openFDA. Public-domain (CC0).