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Anastrozole - 0904-6229-61 - (Anastrozole)

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Drug Information of Anastrozole

Product NDC: 0904-6229
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: 0904-6229
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079220
Marketing Category: ANDA
Start Marketing Date: 20101226

Package Information of Anastrozole

Package NDC: 0904-6229-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-6229-61)

NDC Information of Anastrozole

NDC Code 0904-6229-61
Proprietary Name Anastrozole
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-6229-61)
Product NDC 0904-6229
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anastrozole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101226
Marketing Category Name ANDA
Labeler Name Major 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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