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Anastrozole - 67877-171-30 - (Anastrozole)

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Drug Information of Anastrozole

Product NDC: 67877-171
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: 67877-171
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079220
Marketing Category: ANDA
Start Marketing Date: 20100628

Package Information of Anastrozole

Package NDC: 67877-171-30
Package Description: 30 TABLET in 1 BOTTLE (67877-171-30)

NDC Information of Anastrozole

NDC Code 67877-171-30
Proprietary Name Anastrozole
Package Description 30 TABLET in 1 BOTTLE (67877-171-30)
Product NDC 67877-171
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 Ascend Laboratories, LLC
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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