Dexmethylphenidate Hydrochloride 27808-0092
Product NDC
27808-0092- Manufacturer
- Cranbury Pharmaceuticals, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- November 30, 2001
- Listing Expires
- December 31, 2026
- Application
- ANDA207901
Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmethylphenidate Hydrochloride | 5 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(1)
100 TABLET in 1 BOTTLE (27808-092-01)