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ANASTROZOLE - 43063-383-15 - (ANASTROZOLE)

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Drug Information of ANASTROZOLE

Product NDC: 43063-383
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: 43063-383
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079220
Marketing Category: ANDA
Start Marketing Date: 20100628

Package Information of ANASTROZOLE

Package NDC: 43063-383-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (43063-383-15)

NDC Information of ANASTROZOLE

NDC Code 43063-383-15
Proprietary Name ANASTROZOLE
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (43063-383-15)
Product NDC 43063-383
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 PD-Rx Pharmaceuticals, Inc.
Substance Name ANASTROZOLE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of ANASTROZOLE


General Information