Finasteride (Page 7 of 7)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0093-7355 -05

Finasteride Tablets USP
5 mg

WARNING: Finasteride should not be used by women or children. Women who are or may potentially be pregnant must not use finasteride. They should also not handle crushed or broken tablets of finasteride. (See accompanying circular.)

Rx only

500 TABLETS

Label 5 mg, 500 Tablets
(click image for full-size original)
FINASTERIDE finasteride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0093-7355
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FINASTERIDE (FINASTERIDE) FINASTERIDE 5 mg
Inactive Ingredients
Ingredient Name Strength
FD&C BLUE NO. 2
INDIGOTINDISULFONATE SODIUM
HYPROMELLOSE 2910 (6 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL 400
POLYETHYLENE GLYCOL 6000
POVIDONE K30
STARCH, CORN
SODIUM LAURYL SULFATE
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
Product Characteristics
Color blue Score no score
Shape OVAL (capsule-shaped) Size 10mm
Flavor Imprint Code 93;7355
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0093-7355-56 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:0093-7355-98 90 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:0093-7355-05 500 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076511 12/15/2006
Labeler — Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 01/2022 Teva Pharmaceuticals USA, Inc.

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