Femara - 0078-0249-15 - (letrozole)

Alphabetical Index


Drug Information of Femara

Product NDC: 0078-0249
Proprietary Name: Femara
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 Femara

Product NDC: 0078-0249
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020726
Marketing Category: NDA
Start Marketing Date: 19970731

Package Information of Femara

Package NDC: 0078-0249-15
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0249-15)

NDC Information of Femara

NDC Code 0078-0249-15
Proprietary Name Femara
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0249-15)
Product NDC 0078-0249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name letrozole
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970731
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name LETROZOLE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of Femara


General Information