Dysport - 99207-500-01 - (botulinum toxin type a)

Alphabetical Index


Drug Information of Dysport

Product NDC: 99207-500
Proprietary Name: Dysport
Non Proprietary Name: botulinum toxin type a
Active Ingredient(s): 300    [USP'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: 99207-500
Labeler Name: Medicis Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125274
Marketing Category: BLA
Start Marketing Date: 20090525

Package Information of Dysport

Package NDC: 99207-500-01
Package Description: 1 VIAL in 1 CARTON (99207-500-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

NDC Information of Dysport

NDC Code 99207-500-01
Proprietary Name Dysport
Package Description 1 VIAL in 1 CARTON (99207-500-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Product NDC 99207-500
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 20090525
Marketing Category Name BLA
Labeler Name Medicis Pharmaceutical Corp
Substance Name BOTULINUM TOXIN TYPE A
Strength Number 300
Strength Unit [USP'U]/1
Pharmaceutical Classes Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA]

Complete Information of Dysport


General Information