Package 70518-2718-0

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2718-0
Digits Only 7051827180
Product NDC 70518-2718
Product ID 70518-2718_4a7e6def-2379-64a5-e063-6394a90a011d
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0)

Marketing

Marketing Status
Marketed Since 2020-05-01
Brand naltrexone hydrochloride
Generic naltrexone hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a7e6def-2379-64a5-e063-6394a90a011d", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["f821dd49-3fa7-4d33-99de-19023ff1ae65"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0)", "package_ndc": "70518-2718-0", "marketing_start_date": "20200501"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "70518-2718_4a7e6def-2379-64a5-e063-6394a90a011d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70518-2718", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALTREXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090356", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20271231"}