NDC 75907-050-01
Methylphenidate Hydrochloride (LA) 20 mg/1
Methylphenidate Hydrochloride · CAPSULE, EXTENDED RELEASE
Methylphenidate Hydrochloride (LA) is a capsule, extended release containing methylphenidate hydrochloride at a strength of 20 mg/1. Manufactured by Dr. Reddy's Laboratories Inc.
Key Facts
- Brand Name
- Methylphenidate Hydrochloride (LA)
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
75907-050-01- NDC Code (Product)
75907-050- Manufacturer
- Dr. Reddy's Laboratories Inc
- Strength
- 20 mg/1
- Dosage Form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA078458
- Marketing Start
- 12/20/2024
Recall History
No Recall HistoryView Full Drug Page
Methylphenidate Hydrochloride (LA) — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.