Package 71335-0493-6

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0493-6
Digits Only 7133504936
Product NDC 71335-0493
Description

180 TABLET in 1 BOTTLE (71335-0493-6)

Marketing

Marketing Status
Marketed Since 2024-08-09
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": "eb6232eb-a7e6-40ae-ada5-54ca950c9e17", "openfda": {"unii": ["229809935B"], "rxcui": ["864718"], "spl_set_id": ["cc79daec-2430-4d17-a37d-5a7ff5bfd883"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0493-1)", "package_ndc": "71335-0493-1", "marketing_start_date": "20180316"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0493-2)", "package_ndc": "71335-0493-2", "marketing_start_date": "20180827"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0493-3)", "package_ndc": "71335-0493-3", "marketing_start_date": "20240809"}, {"sample": false, "description": "112 TABLET in 1 BOTTLE (71335-0493-4)", "package_ndc": "71335-0493-4", "marketing_start_date": "20240809"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0493-5)", "package_ndc": "71335-0493-5", "marketing_start_date": "20240809"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0493-6)", "package_ndc": "71335-0493-6", "marketing_start_date": "20240809"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0493-7)", "package_ndc": "71335-0493-7", "marketing_start_date": "20240809"}], "brand_name": "Methadone Hydrochloride", "product_id": "71335-0493_eb6232eb-a7e6-40ae-ada5-54ca950c9e17", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-0493", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203502", "marketing_category": "ANDA", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}