HUMAN PRESCRIPTION DRUG: 47335-714

Brand Name: Finasteride

Generic Name: Finasteride

Primary Class: 5-alpha Reductase Inhibitor [EPC]

SPL Set ID: abd87058-923f-4767-986c-278201c0e688 view on Dailymed | RXCUI: 200172

Manufacturer Name: Sun Pharmaceutical Industries, Inc.

Associated Package NDCs
Package NDC Description
47335-714-08 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)
47335-714-18 1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)
47335-714-81 90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)
47335-714-83 30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)
47335-714-88 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)