Dysport - 15054-0530-6 - (Botulinum Toxin Type A)

Alphabetical Index


Drug Information of Dysport

Product NDC: 15054-0530
Proprietary Name: Dysport
Non Proprietary Name: Botulinum Toxin Type A
Active Ingredient(s): 300    U/1 & nbsp;   Botulinum Toxin Type A
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dysport

Product NDC: 15054-0530
Labeler Name: Ipsen Biopharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125274
Marketing Category: BLA
Start Marketing Date: 20091102

Package Information of Dysport

Package NDC: 15054-0530-6
Package Description: 1 VIAL in 1 CARTON (15054-0530-6) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

NDC Information of Dysport

NDC Code 15054-0530-6
Proprietary Name Dysport
Package Description 1 VIAL in 1 CARTON (15054-0530-6) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Product NDC 15054-0530
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Botulinum Toxin Type A
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20091102
Marketing Category Name BLA
Labeler Name Ipsen Biopharmaceuticals, Inc.
Substance Name BOTULINUM TOXIN TYPE A
Strength Number 300
Strength Unit U/1
Pharmaceutical Classes Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA]

Complete Information of Dysport


General Information