Armodafinil
- Product NDC
- 68180-573
- 11-digit product format
- 681800573
- Labeler code
- 68180
- Product ID
- 68180-573_b4c0895d-90c6-4624-98fb-978e2c2893e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Armodafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA200751
- Marketing category
- ANDA
- Marketing start
- 2016-11-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-573-02 | 68180057302 | 500 TABLET in 1 BOTTLE (68180-573-02) | 500 tablet | 2016-11-28 | 0000-00-00 | No | No | Current |
| 68180-573-07 | 68180057307 | 60 TABLET in 1 BOTTLE (68180-573-07) | 60 tablet | 2016-11-28 | 0000-00-00 | No | No | Current |