Methylphenidate Hydrochloride 10702-0101
Product NDC
10702-0101- Manufacturer
- Kvk-Tech, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- May 11, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA206932
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methylphenidate Hydrochloride | 10 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(1)
100 TABLET in 1 BOTTLE (10702-101-01)