Methylphenidate Hydrochloride 57664-0609
Product NDC
57664-0609- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- August 20, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA205135
Active Ingredients
| Ingredient | Strength |
|---|---|
| Methylphenidate Hydrochloride | 54 mg/1 |
Drug Class
Central Nervous System Stimulant [EPC]Central Nervous System Stimulation [PE]
Packaging Options(1)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-609-88)