Modafinil 69452-0343
Product NDC
69452-0343- Manufacturer
- Bionpharma Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 28, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA078963
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, PLASTIC (69452-343-13)
90 TABLET in 1 BOTTLE, PLASTIC (69452-343-19)
100 TABLET in 1 BOTTLE, PLASTIC (69452-343-20)