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ANASTROZOLE - 51991-620-10 - (ANASTROZOLE)

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Drug Information of ANASTROZOLE

Product NDC: 51991-620
Proprietary Name: ANASTROZOLE
Non Proprietary Name: ANASTROZOLE
Active Ingredient(s): 1    mg/1 & nbsp;   ANASTROZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ANASTROZOLE

Product NDC: 51991-620
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079220
Marketing Category: ANDA
Start Marketing Date: 20100628

Package Information of ANASTROZOLE

Package NDC: 51991-620-10
Package Description: 1000 TABLET in 1 BOTTLE (51991-620-10)

NDC Information of ANASTROZOLE

NDC Code 51991-620-10
Proprietary Name ANASTROZOLE
Package Description 1000 TABLET in 1 BOTTLE (51991-620-10)
Product NDC 51991-620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ANASTROZOLE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100628
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name ANASTROZOLE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of ANASTROZOLE


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