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Dysport
Dysport - 99207-500-01 - (botulinum toxin type a)
Drug Information of Dysport
| Product NDC: | 99207-500 |
| Proprietary Name: | Dysport |
| Non Proprietary Name: | botulinum toxin type a |
| Active Ingredient(s): | 300 [USP'U]/1 & nbsp; botulinum toxin type a |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dysport
| Product NDC: | 99207-500 |
| Labeler Name: | Medicis Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125274 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20090525 |
Package Information of Dysport
| Package NDC: | 99207-500-01 |
| Package Description: | 1 VIAL in 1 CARTON (99207-500-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
NDC Information of Dysport
| NDC Code | 99207-500-01 |
| Proprietary Name | Dysport |
| Package Description | 1 VIAL in 1 CARTON (99207-500-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
| Product NDC | 99207-500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | botulinum toxin type a |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20090525 |
| Marketing Category Name | BLA |
| Labeler Name | Medicis Pharmaceutical Corp |
| Substance Name | BOTULINUM TOXIN TYPE A |
| Strength Number | 300 |
| Strength Unit | [USP'U]/1 |
| Pharmaceutical Classes | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |
