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Anastrozole - 0115-1261-01 - (Anastrozole)

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Drug Information of Anastrozole

Product NDC: 0115-1261
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: 0115-1261
Labeler Name: Global Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA091242
Marketing Category: NDA
Start Marketing Date: 20130605

Package Information of Anastrozole

Package NDC: 0115-1261-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0115-1261-01)

NDC Information of Anastrozole

NDC Code 0115-1261-01
Proprietary Name Anastrozole
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0115-1261-01)
Product NDC 0115-1261
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anastrozole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130605
Marketing Category Name NDA
Labeler Name Global Pharmaceuticals
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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