NDCFind

Finasteride 47335-0714-88

Package NDC

47335-0714-88

Product NDC: 47335-0714

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 23, 2022
Listing Expires
December 31, 2026
Application
ANDA090508
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Active Ingredients

IngredientStrength
Finasteride1 mg/1

Drug Class

5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitors [MoA]

Selected Package

47335-0714-88Selected

100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)

Other packages for this product(4)

100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)

1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)

90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)

30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)