Anastrozole (Page 10 of 10)

Principal Display Panel

NDC: 70934-488-10

Label
(click image for full-size original)
ANASTROZOLE
anastrozole tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70934-488(NDC:16729-035)
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
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (5 MPA.S)
POLYETHYLENE GLYCOL 300
POVIDONE
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
Product Characteristics
Color white Score no score
Shape ROUND (round biconvex) Size 6mm
Flavor Imprint Code AHI
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70934-488-10 10 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090568 01/08/2020
Labeler — Denton Pharma, Inc. DBA Northwind Pharmaceuticals (080355546)
Registrant — Denton Pharma, Inc. DBA Northwind Pharmaceuticals (080355546)
Establishment
Name Address ID/FEI Operations
Denton Pharma, Inc. DBA Northwind Pharmaceuticals 080355546 repack (70934-488)

Revised: 01/2020 Denton Pharma, Inc. DBA Northwind Pharmaceuticals

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