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ANASTROZOLE - 62756-250-83 - (ANASTROZOLE)

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Drug Information of ANASTROZOLE

Product NDC: 62756-250
Proprietary Name: ANASTROZOLE
Non Proprietary Name: ANASTROZOLE
Active Ingredient(s): 1    mg/1 & nbsp;   ANASTROZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ANASTROZOLE

Product NDC: 62756-250
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091177
Marketing Category: ANDA
Start Marketing Date: 20100716

Package Information of ANASTROZOLE

Package NDC: 62756-250-83
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (62756-250-83)

NDC Information of ANASTROZOLE

NDC Code 62756-250-83
Proprietary Name ANASTROZOLE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (62756-250-83)
Product NDC 62756-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ANASTROZOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100716
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name ANASTROZOLE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of ANASTROZOLE


General Information