NDC 57664-229-18
Methylphenidate Hydrochloride 10 mg/1
Methylphenidate Hydrochloride · TABLET
Methylphenidate Hydrochloride is a tablet containing methylphenidate hydrochloride at a strength of 10 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Methylphenidate Hydrochloride
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
57664-229-18- NDC Code (Product)
57664-229- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 10 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA090710
- Marketing Start
- 08/16/2013
Recall History
No Recall HistoryView Full Drug Page
Methylphenidate Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.