Modafinil 71610-0991
Product NDC
71610-0991- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- September 14, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA209966
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 (71610-991-30)
60 TABLET in 1 BOTTLE (71610-991-53)
90 TABLET in 1 BOTTLE (71610-991-60)