Letrozole - 55111-646-78 - (Letrozole)

Alphabetical Index


Drug Information of Letrozole

Product NDC: 55111-646
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: 55111-646
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091191
Marketing Category: ANDA
Start Marketing Date: 20110603

Package Information of Letrozole

Package NDC: 55111-646-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-646-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-646-79)

NDC Information of Letrozole

NDC Code 55111-646-78
Proprietary Name Letrozole
Package Description 10 BLISTER PACK in 1 CARTON (55111-646-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-646-79)
Product NDC 55111-646
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 Dr. Reddy's Laboratories 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