Dexmethylphenidate Hydrochloride 57664-0378-13
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- September 26, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA201231
Active Ingredients
| Ingredient | Strength |
|---|---|
| Dexmethylphenidate Hydrochloride | 5 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Selected Package
57664-0378-13Selected500 TABLET in 1 BOTTLE (57664-378-13)
Other packages for this product(4)
100 TABLET in 1 BOTTLE (57664-378-08)
1000 TABLET in 1 BOTTLE (57664-378-18)
30 TABLET in 1 BOTTLE (57664-378-83)
100 TABLET in 1 BOTTLE (57664-378-88)