Modafinil 46708-0386
Product NDC
46708-0386- Manufacturer
- Alembic Pharmaceuticals Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- June 30, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA202700
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(5)
100 TABLET in 1 CARTON (46708-386-10)
30 TABLET in 1 BOTTLE (46708-386-30)
60 TABLET in 1 BOTTLE (46708-386-60)
90 TABLET in 1 BOTTLE (46708-386-90)
1000 TABLET in 1 BOTTLE (46708-386-91)