Package 64850-300-30

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64850-300-30
Digits Only 6485030030
Product NDC 64850-300
Product ID 64850-300_cae1ac14-ab22-42d1-8449-5e36c137b905
Description

30 TABLET, FILM COATED in 1 BOTTLE (64850-300-30)

Marketing

Marketing Status
Marketed Since 2025-08-15
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naltrexone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cae1ac14-ab22-42d1-8449-5e36c137b905", "openfda": {"upc": ["0364850300018", "0364850300308"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["5f188bdc-2009-43aa-ad32-f06dbfac2642"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (64850-300-01)", "package_ndc": "64850-300-01", "marketing_start_date": "20250815"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (64850-300-30)", "package_ndc": "64850-300-30", "marketing_start_date": "20250815"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "64850-300_cae1ac14-ab22-42d1-8449-5e36c137b905", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "64850-300", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075274", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}