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Anastrozole - 68382-209-10 - (Anastrozole)

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Drug Information of Anastrozole

Product NDC: 68382-209
Proprietary Name: Anastrozole
Non Proprietary Name: Anastrozole
Active Ingredient(s): 1    mg/1 & nbsp;   Anastrozole
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Anastrozole

Product NDC: 68382-209
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078921
Marketing Category: ANDA
Start Marketing Date: 20100627

Package Information of Anastrozole

Package NDC: 68382-209-10
Package Description: 1000 TABLET, COATED in 1 BOTTLE (68382-209-10)

NDC Information of Anastrozole

NDC Code 68382-209-10
Proprietary Name Anastrozole
Package Description 1000 TABLET, COATED in 1 BOTTLE (68382-209-10)
Product NDC 68382-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anastrozole
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100627
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name ANASTROZOLE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of Anastrozole


General Information