Modafinil 71610-0873
Product NDC
71610-0873- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 15, 2019
- Listing Expires
- December 31, 2026
- 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(4)
30 TABLET in 1 BOTTLE (71610-873-30)
60 TABLET in 1 BOTTLE (71610-873-53)
90 TABLET in 1 BOTTLE (71610-873-60)
180 TABLET in 1 BOTTLE (71610-873-80)