Fusilev - 68152-101-00 - (levoleucovorin)

Alphabetical Index


Drug Information of Fusilev

Product NDC: 68152-101
Proprietary Name: Fusilev
Non Proprietary Name: levoleucovorin
Active Ingredient(s): 50    mg/5mL & nbsp;   levoleucovorin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fusilev

Product NDC: 68152-101
Labeler Name: Spectrum Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020140
Marketing Category: NDA
Start Marketing Date: 20080815

Package Information of Fusilev

Package NDC: 68152-101-00
Package Description: 1 VIAL in 1 CARTON (68152-101-00) > 5 mL in 1 VIAL

NDC Information of Fusilev

NDC Code 68152-101-00
Proprietary Name Fusilev
Package Description 1 VIAL in 1 CARTON (68152-101-00) > 5 mL in 1 VIAL
Product NDC 68152-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levoleucovorin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080815
Marketing Category Name NDA
Labeler Name Spectrum Pharmaceuticals, Inc.
Substance Name LEVOLEUCOVORIN CALCIUM
Strength Number 50
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Fusilev


General Information