NDC 0527-3312-37
Methylphenidate Hydrochloride 36 mg/1
Methylphenidate Hydrochloride · TABLET, EXTENDED RELEASE
Methylphenidate Hydrochloride is a tablet, extended release containing methylphenidate hydrochloride at a strength of 36 mg/1. Manufactured by Lannett Company, Inc..
Key Facts
- Brand Name
- Methylphenidate Hydrochloride
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
0527-3312-37- NDC Code (Product)
0527-3312- Manufacturer
- Lannett Company, Inc.
- Strength
- 36 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA211918
- Marketing Start
- 04/24/2019
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.