NDC 57664-378-18
Dexmethylphenidate hydrochloride 5 mg/1
Dexmethylphenidate hydrochloride · TABLET
Dexmethylphenidate hydrochloride is a tablet containing dexmethylphenidate hydrochloride at a strength of 5 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Dexmethylphenidate hydrochloride
- Generic Name
- Dexmethylphenidate hydrochloride
- NDC Code (Package)
57664-378-18- NDC Code (Product)
57664-378- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA201231
- Marketing Start
- 09/26/2013
Recall History
No Recall HistoryView Full Drug Page
Dexmethylphenidate hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.