NDC 55466-103-12
Methylphenidate Hydrochloride 20 mg/1
Methylphenidate Hydrochloride · TABLET
Methylphenidate Hydrochloride is a tablet containing methylphenidate hydrochloride at a strength of 20 mg/1. Manufactured by Neolpharma, Inc..
Key Facts
- Brand Name
- Methylphenidate Hydrochloride
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
55466-103-12- NDC Code (Product)
55466-103- Manufacturer
- Neolpharma, Inc.
- Strength
- 20 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA208737
- Marketing Start
- 03/29/2024
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.