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Neupro
Neupro - 50474-808-11 - (rotigotine)
Drug Information of Neupro
| Product NDC: | 50474-808 |
| Proprietary Name: | Neupro |
| Non Proprietary Name: | rotigotine |
| Active Ingredient(s): | & nbsp; rotigotine |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neupro
| Product NDC: | 50474-808 |
| 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: | 50474-808-11 |
| Package Description: | 2 BOX in 1 KIT (50474-808-11) > 1 KIT in 1 BOX * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
NDC Information of Neupro
| NDC Code | 50474-808-11 |
| Proprietary Name | Neupro |
| Package Description | 2 BOX in 1 KIT (50474-808-11) > 1 KIT in 1 BOX * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH * 7 POUCH in 1 BOX > 1 PATCH in 1 POUCH > 24 h in 1 PATCH |
| Product NDC | 50474-808 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rotigotine |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120402 |
| Marketing Category Name | NDA |
| Labeler Name | UCB, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
