# Methadone Hydrochloride

NDC: 0641-6266
Generic name: Methadone Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20250612

FDA application: ANDA218609

## Active ingredients

- METHADONE HYDROCHLORIDE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6266"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6266
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a6dbcb0-68f2-4f8b-94ee-baa2aa296293