# Dexmethylphenidate Hydrochloride

NDC: 63629-2176
Generic name: Dexmethylphenidate Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170105

FDA application: ANDA202842

## Active ingredients

- DEXMETHYLPHENIDATE HYDROCHLORIDE: 35 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2176"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2176
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06bcef7a-b321-4dd8-9bf6-5d8f8940f04a