Dexmethylphenidate Hydrochloride 67877-0656
Product NDC
67877-0656- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- July 21, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA212631
Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmethylphenidate Hydrochloride | 5 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(3)
100 TABLET in 1 BOTTLE (67877-656-01)
500 TABLET in 1 BOTTLE (67877-656-05)
30 TABLET in 1 BOTTLE (67877-656-30)