Modafinil 70771-1052
Product NDC
70771-1052- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- January 4, 2018
- 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(3)
100 TABLET in 1 BOTTLE (70771-1052-1)
30 TABLET in 1 BOTTLE (70771-1052-3)
90 TABLET in 1 BOTTLE (70771-1052-9)