Prescription Drug Information: Anastrozole (Page 6 of 6)

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Anastrozole Tablets, 1mg, 30 Tablets

NDC 68001-155-04

Anastrozole Tablets USP 1 mg 30ct Rev 1219
(click image for full-size original)
ANASTROZOLE anastrozole tablet, coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68001-155
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, UNSPECIFIED
LACTOSE, UNSPECIFIED FORM
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL, UNSPECIFIED
SODIUM STARCH GLYCOLATE TYPE A POTATO
POVIDONE, UNSPECIFIED
TITANIUM DIOXIDE
Product Characteristics
Color WHITE (WHITE) Score no score
Shape ROUND (ROUND) Size 6mm
Flavor Imprint Code A7
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68001-155-04 30 TABLET, COATED in 1 BOTTLE None
2 NDC:68001-155-08 1000 TABLET, COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078921 01/01/2014
Labeler — BluePoint Laboratories (985523874)
Registrant — Zydus Pharmaceuticals (USA) Inc. (156861945)
Establishment
Name Address ID/FEI Operations
Cadila Healthcare Limited 918596198 ANALYSIS (68001-155), MANUFACTURE (68001-155)

Revised: 01/2020 BluePoint Laboratories

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