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Tolterodine Tartrate

NDC 0093-7164 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079141
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsTOLTERODINE TARTRATE (4 mg/1)
Marketing started20170320
Package count3

External sources

Source: openFDA. Public-domain (CC0).