# Methylphenidate Hydrochloride

NDC: 31722-928
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20180301

FDA application: ANDA210354

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-928"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-928
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb73cd3e-aa7c-4f7e-826d-75e71fb6d1e0