# Dexmethylphenidate Hydrochloride Extended-Release

NDC: 0781-2730
Generic name: dexmethylphenidate hydrochloride
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: NDA AUTHORIZED GENERIC
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260924

FDA application: NDA021802

## Active ingredients

- DEXMETHYLPHENIDATE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-2730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-2730