# Dexmethylphenidate Hydrochloride Extended-Release

NDC: 72162-1502
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: 20131119

FDA application: ANDA078992

## Active ingredients

- DEXMETHYLPHENIDATE HYDROCHLORIDE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32b3c189-f0f8-4f3e-87da-ce56f583fc42