Modafinil 68084-0721
Product NDC
68084-0721- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- June 2, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202566
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(1)
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-721-21) / 1 TABLET in 1 BLISTER PACK (68084-721-11)