Armodafinil
- Product NDC
- 63629-7403
- 11-digit product format
- 636297403
- Labeler code
- 63629
- Product ID
- 63629-7403_5e3528e1-ba26-4daa-963b-622f0ebb8477
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Armodafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021875
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-11-29
- Marketing end
- 0000-00-00
- Substance
- ARMODAFINIL
- Active strength
- 250 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7403-1 | 63629740301 | 30 TABLET in 1 BOTTLE (63629-7403-1) | 30 tablet | 2017-10-04 | 0000-00-00 | No | No | Current |
| 63629-7403-2 | 63629740302 | 28 TABLET in 1 BOTTLE (63629-7403-2) | 28 tablet | 2017-10-04 | 0000-00-00 | No | No | Current |
| 63629-7403-3 | 63629740303 | 90 TABLET in 1 BOTTLE (63629-7403-3) | 90 tablet | 2017-10-04 | 0000-00-00 | No | No | Current |