Modafinil
- Product NDC
- 68788-7432
- 11-digit product format
- 687887432
- Labeler code
- 68788
- Product ID
- 68788-7432_1f084deb-1301-4f58-9268-78fbca50f04a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202566
- Marketing category
- ANDA
- Marketing start
- 2012-09-27
- Marketing end
- 0000-00-00
- Substance
- MODAFINIL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Central Nervous System Stimulation [PE], Increased Sympathetic Activity [PE], Sympathomimetic-like Agent [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-7432-3 | 68788743203 | 30 TABLET in 1 BOTTLE (68788-7432-3) | 30 tablet | 2019-10-03 | 0000-00-00 | No | No | Current |
| 68788-7432-6 | 68788743206 | 60 TABLET in 1 BOTTLE (68788-7432-6) | 60 tablet | 2019-10-03 | 0000-00-00 | No | No | Current |
| 68788-7432-9 | 68788743209 | 90 TABLET in 1 BOTTLE (68788-7432-9) | 90 tablet | 2019-10-03 | 0000-00-00 | No | No | Current |