# METHADONE HYDROCHLORIDE

NDC: 0054-0709
Generic name: METHADONE HYDROCHLORIDE
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19830308

FDA application: ANDA088109

## Active ingredients

- METHADONE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50f14803-78c0-4d19-8b5d-9a9c17582ac1