# Dexmethylphenidate hydrochloride

NDC: 0115-1683
Generic name: Dexmethylphenidate 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: 20150806

FDA application: ANDA079108

## Active ingredients

- DEXMETHYLPHENIDATE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-1683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5312f2c3-bd73-4d29-b8d1-e989282be750