LETROZOLE - 62756-511-18 - (LETROZOLE)

Alphabetical Index


Drug Information of LETROZOLE

Product NDC: 62756-511
Proprietary Name: LETROZOLE
Non Proprietary Name: LETROZOLE
Active Ingredient(s): 2.5    mg/1 & nbsp;   LETROZOLE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of LETROZOLE

Product NDC: 62756-511
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091466
Marketing Category: ANDA
Start Marketing Date: 20110603

Package Information of LETROZOLE

Package NDC: 62756-511-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (62756-511-18)

NDC Information of LETROZOLE

NDC Code 62756-511-18
Proprietary Name LETROZOLE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (62756-511-18)
Product NDC 62756-511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LETROZOLE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110603
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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