Modafinil 71610-0685
Product NDC
71610-0685- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 3, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA077667
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(2)
30 TABLET in 1 BOTTLE (71610-685-30)
60 TABLET in 1 BOTTLE (71610-685-53)