# Methylphenidate Hydrochloride (LA)

NDC: 0093-5347
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20120716

FDA application: ANDA079031

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-5347"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-5347
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=034fb7cd-e183-475e-8beb-64fd88facc8f