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Tamsulosin Hydrochloride

NDC 65841-695 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078225
Dosage form / routeCAPSULE · ORAL
Active ingredientsTAMSULOSIN HYDROCHLORIDE (.4 mg/1)
Marketing started20100427
Package count7

External sources

Source: openFDA. Public-domain (CC0).