Package 71335-0014-4

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0014-4
Digits Only 7133500144
Product NDC 71335-0014
Product ID 71335-0014_55b327a1-8549-45f7-8b82-f09a20373e42
Description

45 TABLET, FILM COATED in 1 BOTTLE (71335-0014-4)

Marketing

Marketing Status
Marketed Since 2017-08-08
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": "55b327a1-8549-45f7-8b82-f09a20373e42", "openfda": {"unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["fa0b0881-97f3-4ca2-bc15-0954293081db"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0014-1)", "package_ndc": "71335-0014-1", "marketing_start_date": "20170808"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0014-2)", "package_ndc": "71335-0014-2", "marketing_start_date": "20170808"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0014-3)", "package_ndc": "71335-0014-3", "marketing_start_date": "20170808"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-0014-4)", "package_ndc": "71335-0014-4", "marketing_start_date": "20170808"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0014-5)", "package_ndc": "71335-0014-5", "marketing_start_date": "20170808"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-0014-6)", "package_ndc": "71335-0014-6", "marketing_start_date": "20170808"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "71335-0014_55b327a1-8549-45f7-8b82-f09a20373e42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71335-0014", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA091205", "marketing_category": "ANDA", "marketing_start_date": "20120118", "listing_expiration_date": "20261231"}