# Methylphenidate

NDC: 10702-164
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20170123

FDA application: ANDA207485

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10702-164"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-164
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2cf1b26b-199d-4c7f-ab64-4805a9def2cc