# Dexmethylphenidate Hydrochloride

NDC: 10702-108
Generic name: Dexmethylphenidate Hydrochloride
Labeler / Manufacturer: KVK-TECH, INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151204

FDA application: ANDA206931

## 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:"10702-108"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-108
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0c717ae4-ec27-47db-ac1b-e504dbb379be