Package 64850-603-01

Brand: methadone hydrochloride

Generic: methadone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64850-603-01
Digits Only 6485060301
Product NDC 64850-603
Product ID 64850-603_6745a13f-b53a-4f0d-9c0a-bbef6343a8d3
Description

100 TABLET in 1 BOTTLE, PLASTIC (64850-603-01)

Marketing

Marketing Status
Marketed Since 2018-08-06
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": "6745a13f-b53a-4f0d-9c0a-bbef6343a8d3", "openfda": {"upc": ["0364850603010", "0364850604017"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["d702d32b-98b1-412d-934c-1cd96af4b95a"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64850-603-01)", "package_ndc": "64850-603-01", "marketing_start_date": "20180806"}], "brand_name": "Methadone Hydrochloride", "product_id": "64850-603_6745a13f-b53a-4f0d-9c0a-bbef6343a8d3", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64850-603", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210484", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}