Modafinil
- Product NDC
- 60429-582
- 11-digit product format
- 604290582
- Labeler code
- 60429
- Product ID
- 60429-582_9d281978-9023-65ee-e053-2a95a90a49cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- modafinil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA077667
- Marketing category
- ANDA
- Marketing start
- 2014-02-03
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| R3UK8X3U3D | MODAFINIL | 68693-11-8 | MODAFINIL |