NDC 0093-5347-01
Methylphenidate Hydrochloride (LA) 30 mg/1
Methylphenidate Hydrochloride · CAPSULE, EXTENDED RELEASE
Methylphenidate Hydrochloride (LA) is a capsule, extended release containing methylphenidate hydrochloride at a strength of 30 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Methylphenidate Hydrochloride (LA)
- Generic Name
- Methylphenidate Hydrochloride
- NDC Code (Package)
0093-5347-01- NDC Code (Product)
0093-5347- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 30 mg/1
- Dosage Form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA079031
- Marketing Start
- 07/16/2012
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.