Package 68094-909-50

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68094-909-50
Digits Only 6809490950
Product NDC 68094-909
Product ID 68094-909_efc0724d-4c6e-4974-928c-fd50774f5980
Description

100 TABLET, FILM COATED in 1 BOTTLE (68094-909-50)

Marketing

Marketing Status
Discontinued 2028-06-30
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": "efc0724d-4c6e-4974-928c-fd50774f5980", "openfda": {"upc": ["0368094909501"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["b09b4b5e-795a-48e7-b7cc-2e29f41c5660"], "manufacturer_name": ["Precision Dose Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68094-909-30)", "package_ndc": "68094-909-30", "marketing_end_date": "20280630", "marketing_start_date": "20240215"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68094-909-50)", "package_ndc": "68094-909-50", "marketing_end_date": "20280630", "marketing_start_date": "20240215"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "68094-909_efc0724d-4c6e-4974-928c-fd50774f5980", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "68094-909", "generic_name": "Naltrexone Hydrochloride", "labeler_name": "Precision Dose Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naltrexone Hydrochloride", "active_ingredients": [{"name": "NALTREXONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075274", "marketing_category": "ANDA", "marketing_end_date": "20280630", "marketing_start_date": "20240215"}