Home
>
National Drug Code (NDC)
>
NUVIGIL
NUVIGIL - 16590-394-30 - (ARMODAFINIL)
Drug Information of NUVIGIL
| Product NDC: | 16590-394 |
| 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: | 16590-394 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021875 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of NUVIGIL
| Package NDC: | 16590-394-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (16590-394-30) |
NDC Information of NUVIGIL
| NDC Code | 16590-394-30 |
| Proprietary Name | NUVIGIL |
| Package Description | 30 TABLET in 1 BOTTLE (16590-394-30) |
| Product NDC | 16590-394 |
| 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 | STAT Rx USA LLC |
| Substance Name | ARMODAFINIL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
