Modafinil 71335-2501
Product NDC
71335-2501- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- February 21, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA207196
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(10)
100 TABLET in 1 BOTTLE, PLASTIC (71335-2501-0)
30 TABLET in 1 BOTTLE, PLASTIC (71335-2501-1)
18 TABLET in 1 BOTTLE, PLASTIC (71335-2501-2)
16 TABLET in 1 BOTTLE, PLASTIC (71335-2501-3)
8 TABLET in 1 BOTTLE, PLASTIC (71335-2501-4)
10 TABLET in 1 BOTTLE, PLASTIC (71335-2501-5)
60 TABLET in 1 BOTTLE, PLASTIC (71335-2501-6)
90 TABLET in 1 BOTTLE, PLASTIC (71335-2501-7)
45 TABLET in 1 BOTTLE, PLASTIC (71335-2501-8)
180 TABLET in 1 BOTTLE, PLASTIC (71335-2501-9)