Armodafinil 72189-0133
Product NDC
72189-0133- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIV
- Marketing Start
- October 15, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA206069
Active Ingredients
| Ingredient | Strength |
|---|---|
| Armodafinil | 250 mg/1 |
Packaging Options(1)
30 TABLET in 1 BOTTLE (72189-133-30)