# Methylphenidate Hydrochloride

NDC: 67877-603
Generic name: Methylphenidate Hydrochloride
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20200401

FDA application: ANDA211647

## Active ingredients

- METHYLPHENIDATE HYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-603"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-603
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5fa3da25-13aa-4ee3-acf5-cd505f4688d0