letrozole - 68382-363-30 - (letrozole)

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Drug Information of letrozole

Product NDC: 68382-363
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: 68382-363
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090405
Marketing Category: ANDA
Start Marketing Date: 20110603

Package Information of letrozole

Package NDC: 68382-363-30
Package Description: 10 BLISTER PACK in 1 CARTON (68382-363-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of letrozole

NDC Code 68382-363-30
Proprietary Name letrozole
Package Description 10 BLISTER PACK in 1 CARTON (68382-363-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 68382-363
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 Zydus Pharmaceuticals (USA) 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