NDC 72865-135-01
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 XLCare Pharmaceuticals, Inc..
Key Facts
- Brand Name
- Methylphenidate Hydrochloride
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
72865-135-01- NDC Code (Product)
72865-135- Manufacturer
- XLCare Pharmaceuticals, Inc.
- Strength
- 36 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA211009
- Marketing Start
- 02/24/2020
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.