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Tolterodine tartrate

NDC 29300-307 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216917
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsTOLTERODINE TARTRATE (4 mg/1)
Marketing started20241001
Package count3

External sources

Source: openFDA. Public-domain (CC0).