LETROZOLE - 51991-759-33 - (LETROZOLE)

Alphabetical Index


Drug Information of LETROZOLE

Product NDC: 51991-759
Proprietary Name: LETROZOLE
Non Proprietary Name: LETROZOLE
Active Ingredient(s): 2.5    mg/1 & nbsp;   LETROZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LETROZOLE

Product NDC: 51991-759
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200161
Marketing Category: ANDA
Start Marketing Date: 20110604

Package Information of LETROZOLE

Package NDC: 51991-759-33
Package Description: 30 TABLET in 1 BOTTLE (51991-759-33)

NDC Information of LETROZOLE

NDC Code 51991-759-33
Proprietary Name LETROZOLE
Package Description 30 TABLET in 1 BOTTLE (51991-759-33)
Product NDC 51991-759
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LETROZOLE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110604
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name LETROZOLE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of LETROZOLE


General Information