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Dutasteride and Tamsulosin Hydrochloride

NDC 10370-280 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202509
Dosage form / routeCAPSULE · ORAL
Active ingredientsDUTASTERIDE (.5 mg/1)
TAMSULOSIN HYDROCHLORIDE (.4 mg/1)
Marketing started20151118
Package count2

External sources

Source: openFDA. Public-domain (CC0).