Finasteride (Page 6 of 6)

FINASTERIDE TABLET, FILM COATED

Label Image
(click image for full-size original)
FINASTERIDE finasteride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50436-0089(NDC:16729-089)
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
LACTOSE MONOHYDRATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL, UNSPECIFIED
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
LAUROYL PEG-32 GLYCERIDES
Product Characteristics
Color brown (REDDISH) Score no score
Shape ROUND Size 7mm
Flavor Imprint Code F1
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50436-0089-1 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:50436-0089-3 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091643 11/08/2013
Labeler — Unit Dose Services (831995316)
Establishment
Name Address ID/FEI Operations
Unit Dose Services 831995316 REPACK (50436-0089), RELABEL (50436-0089)

Revised: 02/2019 Unit Dose Services

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