Anastrozole (Page 7 of 7)

Package/Label Display Panel

1mg
(click image for full-size original)

90
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ANASTROZOLE
anastrozole tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42291-085(NDC:0093-7536)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ANASTROZOLE (ANASTROZOLE) ANASTROZOLE 1 mg
Inactive Ingredients
Ingredient Name Strength
HYPROMELLOSE 2910 (5 MPA.S)
LACTOSE MONOHYDRATE
POLYETHYLENE GLYCOL 400
POLYETHYLENE GLYCOL 6000
MAGNESIUM STEARATE
POVIDONE K30
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
Product Characteristics
Color white (white to off-white) Score no score
Shape ROUND Size 6mm
Flavor Imprint Code TEVA;A10
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:42291-085-30 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:42291-085-90 90 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078058 03/13/2020
Labeler — AvKARE (796560394)

Revised: 01/2024 AvKARE

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