Package 0406-6225-05

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0406-6225-05
Digits Only 0406622505
Product NDC 0406-6225
Product ID 0406-6225_56ffbe46-c151-4fe4-af5d-c408311c261f
Description

500 mL in 1 BOTTLE (0406-6225-05)

Marketing

Marketing Status
Marketed Since 2021-06-18
Brand methadone hydrochloride
Generic methadone hydrochloride
Sample Package No

Linked Drug Pages (1)

METHADONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56ffbe46-c151-4fe4-af5d-c408311c261f", "openfda": {"upc": ["0304066221059", "0304066225057"], "unii": ["229809935B"], "rxcui": ["864761", "864769"], "spl_set_id": ["5baef1bf-8bf0-429c-a4ce-1c93171f3f15"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE (0406-6225-05)", "package_ndc": "0406-6225-05", "marketing_start_date": "20210618"}], "brand_name": "METHADONE HYDROCHLORIDE", "product_id": "0406-6225_56ffbe46-c151-4fe4-af5d-c408311c261f", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-6225", "dea_schedule": "CII", "generic_name": "METHADONE HYDROCHLORIDE", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHADONE HYDROCHLORIDE", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA207537", "marketing_category": "ANDA", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}