# Methadone Hydrochloride

NDC: 17856-0392
Generic name: Methadone Hydrochloride
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CONCENTRATE
Routes: ORAL
Marketing started: 20190514

FDA application: ANDA040180

## 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:"17856-0392"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0392
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7b30c78-c531-4dc5-9552-d68daa3210d1