# DEXMETHYLPHENIDATE HYDROCHLORIDE

NDC: 31722-232
Generic name: dexmethylphenidate hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20211208

FDA application: ANDA215523

## 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:"31722-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=77659abe-74be-4092-90fe-cc475726d4ec