Package 62135-242-30

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-242-30
Digits Only 6213524230
Product NDC 62135-242
Product ID 62135-242_1adc57cf-70f9-75b9-e063-6294a90a0de0
Description

30 TABLET, FILM COATED in 1 BOTTLE (62135-242-30)

Marketing

Marketing Status
Marketed Since 2022-01-05
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": "1adc57cf-70f9-75b9-e063-6294a90a0de0", "openfda": {"upc": ["0362135242909", "0362135242602", "0362135242305"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["adb7c4dc-221a-4d91-9687-0d78913a92ad"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62135-242-30)", "package_ndc": "62135-242-30", "marketing_start_date": "20220105"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62135-242-60)", "package_ndc": "62135-242-60", "marketing_start_date": "20240611"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-242-90)", "package_ndc": "62135-242-90", "marketing_start_date": "20220105"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "62135-242_1adc57cf-70f9-75b9-e063-6294a90a0de0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "62135-242", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA207905", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}