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Neupro
Neupro - 50474-803-17 - (rotigotine)
Drug Information of Neupro
| Product NDC: | 50474-803 |
| Proprietary Name: | Neupro |
| Non Proprietary Name: | rotigotine |
| Active Ingredient(s): | 3 mg/24h & nbsp; rotigotine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neupro
| Product NDC: | 50474-803 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021829 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120402 |
Package Information of Neupro
| Package NDC: | 50474-803-17 |
| Package Description: | 7 POUCH in 1 CARTON (50474-803-17) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
NDC Information of Neupro
| NDC Code | 50474-803-17 |
| Proprietary Name | Neupro |
| Package Description | 7 POUCH in 1 CARTON (50474-803-17) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
| Product NDC | 50474-803 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rotigotine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20120402 |
| Marketing Category Name | NDA |
| Labeler Name | UCB, Inc. |
| Substance Name | ROTIGOTINE |
| Strength Number | 3 |
| Strength Unit | mg/24h |
| Pharmaceutical Classes |
