Package 0054-3553-44

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-3553-44
Digits Only 0054355344
Product NDC 0054-3553
Product ID 0054-3553_f4843a89-4cfb-40de-8399-a7449b4865e2
Description

1 BOTTLE in 1 CARTON (0054-3553-44) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 1988-09-06
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": "f4843a89-4cfb-40de-8399-a7449b4865e2", "openfda": {"unii": ["229809935B"], "rxcui": ["991147"], "spl_set_id": ["d0e6a966-179a-45e0-8444-4c1b8523f8d2"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0054-3553-44)  / 30 mL in 1 BOTTLE", "package_ndc": "0054-3553-44", "marketing_start_date": "19880906"}], "brand_name": "Methadone Hydrochloride", "product_id": "0054-3553_f4843a89-4cfb-40de-8399-a7449b4865e2", "dosage_form": "CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-3553", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA089897", "marketing_category": "ANDA", "marketing_start_date": "19880906", "listing_expiration_date": "20261231"}