# Methylphenidate Hydrochloride

NDC: 57664-710
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20241220

FDA application: ANDA217229

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 72 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-710"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-710
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=18024571-4505-6d51-e063-6294a90a1972