Modafinil 23155-0604
Product NDC
23155-0604- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 18, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA207196
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(4)
100 TABLET in 1 BOTTLE, PLASTIC (23155-604-01)
30 TABLET in 1 BOTTLE, PLASTIC (23155-604-03)
500 TABLET in 1 BOTTLE, PLASTIC (23155-604-05)
90 TABLET in 1 BOTTLE, PLASTIC (23155-604-09)