# Methylphenidate Hydrochloride

NDC: 50268-545
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210422

FDA application: ANDA211009

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 18 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50268-545"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-545
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c0906610-294d-1320-e053-2995a90ad8fd