HUMAN PRESCRIPTION DRUG: 47335-715

Brand Name: FINASTERIDE

Generic Name: FINASTERIDE

Primary Class: 5-alpha Reductase Inhibitor [EPC]

SPL Set ID: f149569c-05d1-4dba-b35a-4ed6a633f776 view on Dailymed | RXCUI: 310346

Manufacturer Name: Sun Pharmaceutical Industries, Inc.

Associated Package NDCs
Package NDC Description
47335-715-08 100 TABLET, FILM COATED in 1 BOTTLE (47335-715-08)
47335-715-13 500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13)
47335-715-18 1000 TABLET, FILM COATED in 1 BOTTLE (47335-715-18)
47335-715-81 90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)
47335-715-83 30 TABLET, FILM COATED in 1 BOTTLE (47335-715-83)
47335-715-88 100 TABLET, FILM COATED in 1 BOTTLE (47335-715-88)