# Methylphenidate Hydrochloride

NDC: 13107-382
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Aurolife Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170411

FDA application: ANDA209276

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13107-382"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13107-382
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=35be77db-fbe3-487e-a220-a08a11aaec28