FDA NDC Directory · JSON-LD · Markdown

Tamsulosin Hydrochloride

NDC 68788-7050 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202433
Dosage form / routeCAPSULE · ORAL
Active ingredientsTAMSULOSIN HYDROCHLORIDE (.4 mg/1)
Marketing started20200601
Package count6

External sources

Source: openFDA. Public-domain (CC0).