NDC Code | 99207-500-30 |
Package Description | 1 VIAL in 1 CARTON (99207-500-30) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Product NDC | 99207-500 |
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 | 20090525 |
End Marketing Date | 20150331 |
Marketing Category Name | BLA |
Application Number | BLA125274 |
Manufacturer | Medicis Pharmaceutical Corp |
Substance Name | BOTULINUM TOXIN TYPE A |
Strength | 300 |
Strength Unit | [USP&apos'U]/1 |
Pharmacy Classes | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |