Finasteride (Page 6 of 6)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 1 mg

NDC 68788-6875
Rx only
Finasteride Tablets USP
1 mg AUROBINDO

Repackaged By: Preferred Pharmaceuticals Inc.

Finasteride Tablets, USP 1mg
(click image for full-size original)
FINASTERIDE finasteride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68788-6875(NDC:65862-927)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FINASTERIDE (FINASTERIDE) FINASTERIDE 1 mg
Inactive Ingredients
Ingredient Name Strength
DOCUSATE SODIUM
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
HYPROMELLOSE 2910 (6 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score no score
Shape OCTAGON (8 sided) (Biconvex) Size 7mm
Flavor Imprint Code J;81
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68788-6875-3 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:68788-6875-6 60 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:68788-6875-9 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203687 01/23/2017
Labeler — Preferred Pharmaceuticals Inc. (791119022)
Registrant — Preferred Pharmaceuticals Inc. (791119022)
Establishment
Name Address ID/FEI Operations
Preferred Pharmaceuticals Inc. 791119022 REPACK (68788-6875)

Revised: 05/2022 Preferred Pharmaceuticals Inc.

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