Package 0904-7036-04

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7036-04
Digits Only 0904703604
Product NDC 0904-7036
Product ID 0904-7036_7464e76f-517a-4fa8-b7ee-86d7071b56d9
Description

30 BLISTER PACK in 1 CARTON (0904-7036-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-02-29
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": "7464e76f-517a-4fa8-b7ee-86d7071b56d9", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["69cb8573-08c1-4957-a768-6cd383f6a3f4"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7036-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7036-04", "marketing_start_date": "20120229"}], "brand_name": "NALTREXONE HYDROCHLORIDE", "product_id": "0904-7036_7464e76f-517a-4fa8-b7ee-86d7071b56d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0904-7036", "generic_name": "NALTREXONE HYDROCHLORIDE", "labeler_name": "Major Pharmaceuticals", "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": "20120229", "listing_expiration_date": "20261231"}