Modafinil 71205-0477
Product NDC
71205-0477- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- September 27, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA202566
Active Ingredients
| Ingredient | Strength |
|---|---|
| Modafinil | 100 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 (71205-477-30)
60 TABLET in 1 BOTTLE (71205-477-60)
90 TABLET in 1 BOTTLE (71205-477-90)