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BOTOX Cosmetic - 0023-9232-01 - (onabotulinumtoxinA)

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Drug Information of BOTOX Cosmetic

Product NDC: 0023-9232
Proprietary Name: BOTOX Cosmetic
Non Proprietary Name: onabotulinumtoxinA
Active Ingredient(s): 100    [USP'U]/1 & nbsp;   onabotulinumtoxinA
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BOTOX Cosmetic

Product NDC: 0023-9232
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103000
Marketing Category: BLA
Start Marketing Date: 20020429

Package Information of BOTOX Cosmetic

Package NDC: 0023-9232-01
Package Description: 1 VIAL, GLASS in 1 CARTON (0023-9232-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS

NDC Information of BOTOX Cosmetic

NDC Code 0023-9232-01
Proprietary Name BOTOX Cosmetic
Package Description 1 VIAL, GLASS in 1 CARTON (0023-9232-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS
Product NDC 0023-9232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name onabotulinumtoxinA
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20020429
Marketing Category Name BLA
Labeler Name Allergan, Inc.
Substance Name BOTULINUM TOXIN TYPE A
Strength Number 100
Strength Unit [USP'U]/1
Pharmaceutical Classes Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA]

Complete Information of BOTOX Cosmetic


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