Modafinil 68788-8653
Product NDC
68788-8653- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- May 9, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA207196
Active Ingredients
| Ingredient | Strength |
|---|---|
| Modafinil | 200 mg/1 |
Drug Class
Sympathomimetic-like Agent [EPC]Central Nervous System Stimulation [PE]Increased Sympathetic Activity [PE]
Packaging Options(3)
30 TABLET in 1 BOTTLE (68788-8653-3)
60 TABLET in 1 BOTTLE (68788-8653-6)
90 TABLET in 1 BOTTLE (68788-8653-9)