Package 42806-318-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-318-01
Digits Only 4280631801
Product NDC 42806-318
Product ID 42806-318_43485290-cdfc-4126-a615-c52745fcd68b
Description

100 TABLET in 1 BOTTLE (42806-318-01)

Marketing

Marketing Status
Marketed Since 2018-06-11
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": "43485290-cdfc-4126-a615-c52745fcd68b", "openfda": {"unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["6da7501b-b881-4bc7-891a-74214a00a3ac"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-318-01)", "package_ndc": "42806-318-01", "marketing_start_date": "20180611"}], "brand_name": "Methadone Hydrochloride", "product_id": "42806-318_43485290-cdfc-4126-a615-c52745fcd68b", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-318", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090065", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}