Home
>
National Drug Code (NDC)
>
Nuvigil
Nuvigil - 0179-0080-70 - (ARMODAFINIL)
Drug Information of Nuvigil
| Product NDC: | 0179-0080 |
| Proprietary Name: | Nuvigil |
| Non Proprietary Name: | ARMODAFINIL |
| Active Ingredient(s): | 250 mg/1 & nbsp; ARMODAFINIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nuvigil
| Product NDC: | 0179-0080 |
| Labeler Name: | KAISER FOUNDATION HOSPITALS |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021875 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110128 |
Package Information of Nuvigil
| Package NDC: | 0179-0080-70 |
| Package Description: | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0080-70) |
NDC Information of Nuvigil
| NDC Code | 0179-0080-70 |
| Proprietary Name | Nuvigil |
| Package Description | 30 TABLET in 1 BOX, UNIT-DOSE (0179-0080-70) |
| Product NDC | 0179-0080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ARMODAFINIL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110128 |
| Marketing Category Name | NDA |
| Labeler Name | KAISER FOUNDATION HOSPITALS |
| Substance Name | ARMODAFINIL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
