# Methadone Hydrochloride

NDC: 67877-660
Generic name: Methadone Hydrochloride
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250701

FDA application: ANDA090635

## Active ingredients

- METHADONE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0366917-f745-4b01-a662-a98a7d80b4a0