Methylphenidate Hydrochloride 57664-0229-08
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- August 16, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA090710
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methylphenidate Hydrochloride | 10 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Selected Package
57664-0229-08Selected100 TABLET in 1 BOTTLE (57664-229-08)
Other packages for this product(4)
500 TABLET in 1 BOTTLE (57664-229-13)
1000 TABLET in 1 BOTTLE (57664-229-18)
30 TABLET in 1 BOTTLE (57664-229-83)
100 TABLET in 1 BOTTLE (57664-229-88)