Dysport (Galderma Laboratories, L.P.)


Welcome to the PulseAid listing for the Dysport drug offered from Galderma Laboratories, L.P.. This Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Galderma Laboratories, L.P.
NON-PROPRIETARY NAME: Botulinum Toxin Type A
SUBSTANCE NAME: BOTULINUM TOXIN TYPE A
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA]
ROUTE: INTRAMUSCULAR
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2009-11-02
END MARKETING DATE: 0000-00-00


Dysport HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDysport from Galderma Laboratories, L.P.
LABELER NAME: Galderma Laboratories, L.P.
DEA SCHEDULE:
ACTIVE STRENGTH: 300(U/1)
START MARKETING DATE: 2009-11-02
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0299-5962_2538f3cc-f8a8-44e2-bebe-7cd8842b7a39
PRODUCT NDC: 0299-5962
APPLICATION NUMBER: BLA125274

Other BOTULINUM TOXIN TYPE A Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.BOTOX
Galderma Laboratories, L.P.Dysport
Ipsen Biopharmaceuticals, Inc.Dysport
Merz North America, Inc.Xeomin
Merz Pharmaceuticals, LLCXeomin