Home
>
National Drug Code (NDC)
>
Dysport
Dysport - 15054-0500-2 - (Botulinum Toxin Type A)
Drug Information of Dysport
| Product NDC: | 15054-0500 |
| Proprietary Name: | Dysport |
| Non Proprietary Name: | Botulinum Toxin Type A |
| Active Ingredient(s): | 500 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: | 15054-0500 |
| Labeler Name: | Ipsen Biopharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA125274 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20091102 |
Package Information of Dysport
| Package NDC: | 15054-0500-2 |
| Package Description: | 2 VIAL in 1 CARTON (15054-0500-2) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
NDC Information of Dysport
| NDC Code | 15054-0500-2 |
| Proprietary Name | Dysport |
| Package Description | 2 VIAL in 1 CARTON (15054-0500-2) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
| Product NDC | 15054-0500 |
| 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 | 20091102 |
| Marketing Category Name | BLA |
| Labeler Name | Ipsen Biopharmaceuticals, Inc. |
| Substance Name | BOTULINUM TOXIN TYPE A |
| Strength Number | 500 |
| Strength Unit | U/1 |
| Pharmaceutical Classes | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |
