Letrozole - 60505-3255-1 - (Letrozole)

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Drug Information of Letrozole

Product NDC: 60505-3255
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: 60505-3255
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091303
Marketing Category: ANDA
Start Marketing Date: 20120531

Package Information of Letrozole

Package NDC: 60505-3255-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60505-3255-1)

NDC Information of Letrozole

NDC Code 60505-3255-1
Proprietary Name Letrozole
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60505-3255-1)
Product NDC 60505-3255
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Letrozole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120531
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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