Methylphenidate 00781-2362
Product NDC
00781-2362- Manufacturer
- Sandoz Inc
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- November 24, 2015
- Application
- NDA021284
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methylphenidate Hydrochloride | 20 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(1)
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2362-01)