Home
>
National Drug Code (NDC)
>
Armodafinil
Armodafinil - 0591-3704-60 - (Armodafinil)
Drug Information of Armodafinil
| Product NDC: | 0591-3704 |
| Proprietary Name: | Armodafinil |
| Non Proprietary Name: | Armodafinil |
| Active Ingredient(s): | 200 mg/1 & nbsp; Armodafinil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Armodafinil
| Product NDC: | 0591-3704 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200156 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120828 |
Package Information of Armodafinil
| Package NDC: | 0591-3704-60 |
| Package Description: | 60 TABLET in 1 BOTTLE, PLASTIC (0591-3704-60) |
NDC Information of Armodafinil
| NDC Code | 0591-3704-60 |
| Proprietary Name | Armodafinil |
| Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (0591-3704-60) |
| Product NDC | 0591-3704 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Armodafinil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120828 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | ARMODAFINIL |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
