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Nuvigil
Nuvigil - 63459-215-30 - (armodafinil)
Drug Information of Nuvigil
| Product NDC: | 63459-215 |
| Proprietary Name: | Nuvigil |
| Non Proprietary Name: | armodafinil |
| Active Ingredient(s): | 150 mg/1 & nbsp; armodafinil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nuvigil
| Product NDC: | 63459-215 |
| Labeler Name: | Cephalon, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021875 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of Nuvigil
| Package NDC: | 63459-215-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (63459-215-30) |
NDC Information of Nuvigil
| NDC Code | 63459-215-30 |
| Proprietary Name | Nuvigil |
| Package Description | 30 TABLET in 1 BOTTLE (63459-215-30) |
| Product NDC | 63459-215 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | armodafinil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | NDA |
| Labeler Name | Cephalon, Inc. |
| Substance Name | ARMODAFINIL |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
