# Methylphenidate Hydrochloride Extended-Release

NDC: 0406-0154
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20121228

FDA application: ANDA202608

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 54 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0406-0154"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-0154
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1b0f2ff-d9df-42ab-b471-226ecf97e075