Cubicin - 67919-011-01 - (Daptomycin)

Alphabetical Index


Drug Information of Cubicin

Product NDC: 67919-011
Proprietary Name: Cubicin
Non Proprietary Name: Daptomycin
Active Ingredient(s): 500    mg/10mL & nbsp;   Daptomycin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cubicin

Product NDC: 67919-011
Labeler Name: Cubist Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021572
Marketing Category: NDA
Start Marketing Date: 20030912

Package Information of Cubicin

Package NDC: 67919-011-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (67919-011-01) > 10 mL in 1 VIAL, SINGLE-USE

NDC Information of Cubicin

NDC Code 67919-011-01
Proprietary Name Cubicin
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (67919-011-01) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC 67919-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Daptomycin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030912
Marketing Category Name NDA
Labeler Name Cubist Pharmaceuticals, Inc.
Substance Name DAPTOMYCIN
Strength Number 500
Strength Unit mg/10mL
Pharmaceutical Classes Lipopeptide Antibacterial [EPC],Lipopeptides [Chemical/Ingredient]

Complete Information of Cubicin


General Information