FDA NDC Directory · JSON-LD · Markdown

tamsulosin hydrochloride

NDC 72865-350 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerXLCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214730
Dosage form / routeCAPSULE · ORAL
Active ingredientsTAMSULOSIN HYDROCHLORIDE (.4 mg/1)
Marketing started20260101
Package count2

External sources

Source: openFDA. Public-domain (CC0).