# Methylphenidate Hydrochloride

NDC: 0115-1739
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160920

FDA application: ANDA205105

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-1739"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1739
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10aa0dc0-bd0e-4927-a19a-8722d78ad67d