# METHYLPHENIDATE HYDROCHLORIDE

NDC: 31722-175
Generic name: METHYLPHENIDATE HYDROCHLORIDE
Labeler / Manufacturer: Camber Pharmaceutical Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151001

FDA application: ANDA207416

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-175"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-175
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=778190da-1528-4def-94bf-ee23ee5268a5