Package 23155-886-01

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 23155-886-01
Digits Only 2315588601
Product NDC 23155-886
Product ID 23155-886_6ffda82d-69f6-40f7-90fd-53b628440934
Description

100 TABLET, FILM COATED in 1 BOTTLE (23155-886-01)

Marketing

Marketing Status
Marketed Since 2023-10-06
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": "6ffda82d-69f6-40f7-90fd-53b628440934", "openfda": {"upc": ["0323155886030", "0323155886016"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["c67a22bb-d2bd-4da5-9d3e-6b5281f10891"], "manufacturer_name": ["Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (23155-886-01)", "package_ndc": "23155-886-01", "marketing_start_date": "20231006"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (23155-886-03)", "package_ndc": "23155-886-03", "marketing_start_date": "20231006"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "23155-886_6ffda82d-69f6-40f7-90fd-53b628440934", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "23155-886", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc", "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": "20231006", "listing_expiration_date": "20261231"}