| NDC Code | 0299-5962-01 | 
|---|
			| Package Description | 1 VIAL in 1 CARTON (0299-5962-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL | 
|---|
			| Product NDC | 0299-5962 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Dysport | 
|---|
			
			| Non-Proprietary Name | Botulinum Toxin Type A | 
|---|
			| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 
|---|
			| Usage | INTRAMUSCULAR | 
|---|
			| Start Marketing Date | 20091102 | 
|---|
			
			| Marketing Category Name | BLA | 
|---|
			| Application Number | BLA125274 | 
|---|
			| Manufacturer | Galderma Laboratories, L.P. | 
|---|
			| Substance Name | BOTULINUM TOXIN TYPE A | 
|---|
			| Strength | 300 | 
|---|
			| Strength Unit | U/1 | 
|---|
			| Pharmacy Classes | Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC] | 
|---|