NDC Code | 0259-4150-01 |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0259-4150-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE |
Product NDC | 0259-4150 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Xeomin |
Non-Proprietary Name | Incobotulinumtoxina |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR |
Start Marketing Date | 20100901 |
Marketing Category Name | BLA |
Application Number | BLA125360 |
Manufacturer | Merz Pharmaceuticals, LLC |
Substance Name | BOTULINUM TOXIN TYPE A |
Strength | 50 |
Strength Unit | [USP'U]/1 |
Pharmacy Classes | Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC] |