Package 17856-0392-6

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17856-0392-6
Digits Only 1785603926
Product NDC 17856-0392
Description

1 SYRINGE in 1 BAG (17856-0392-6) / .5 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2025-05-30
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36b0bbb0-eb9e-7547-e063-6394a90a25f4", "openfda": {"unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["d7b30c78-c531-4dc5-9552-d68daa3210d1"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "60 SYRINGE in 1 BOX, UNIT-DOSE (17856-0392-1)  / .5 mL in 1 SYRINGE", "package_ndc": "17856-0392-1", "marketing_start_date": "20240520"}, {"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0392-3)  / 2.5 mL in 1 CUP, UNIT-DOSE (17856-0392-4)", "package_ndc": "17856-0392-3", "marketing_start_date": "20240520"}, {"sample": false, "description": "1 SYRINGE in 1 BAG (17856-0392-6)  / .5 mL in 1 SYRINGE", "package_ndc": "17856-0392-6", "marketing_start_date": "20250530"}, {"sample": false, "description": "5 BOX, UNIT-DOSE in 1 SYRINGE (17856-0392-7)  / 60 SYRINGE in 1 BOX, UNIT-DOSE (17856-0392-2)  / 1 mL in 1 SYRINGE (17856-0392-5)", "package_ndc": "17856-0392-7", "marketing_start_date": "20240520"}, {"sample": false, "description": "1 SYRINGE in 1 BAG (17856-0392-8)  / 1 mL in 1 SYRINGE", "package_ndc": "17856-0392-8", "marketing_start_date": "20250530"}, {"sample": false, "description": "1 SYRINGE in 1 BAG (17856-0392-9)  / 2.5 mL in 1 SYRINGE", "package_ndc": "17856-0392-9", "marketing_start_date": "20250530"}], "brand_name": "Methadone Hydrochloride", "product_id": "17856-0392_36b0bbb0-eb9e-7547-e063-6394a90a25f4", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "17856-0392", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA040180", "marketing_category": "ANDA", "marketing_start_date": "20190514", "listing_expiration_date": "20261231"}