Armodafinil
- Product NDC
- 0591-3856
- 11-digit product format
- 005913856
- Labeler code
- 0591
- Product ID
- 0591-3856_af7e1991-df84-461f-bb39-b8daeb5fa0b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Armodafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- NDA021875
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-06-01
- Marketing end
- 2021-05-31
- Substance
- ARMODAFINIL
- Active strength
- 200 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-3856-30 | 00591385630 | 30 TABLET in 1 BOTTLE (0591-3856-30) | 30 tablet | 2016-06-01 | 2021-05-31 | No | No | Current |