Dexmethylphenidate Hydrochloride 43386-0862
Product NDC
43386-0862- Manufacturer
- Lupin Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- December 4, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA204534
Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmethylphenidate Hydrochloride | 2.5 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(1)
100 TABLET in 1 BOTTLE (43386-862-01)