Package 68094-853-61

Brand: naltrexone hydrochloride

Generic: naltrexone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68094-853-61
Digits Only 6809485361
Product NDC 68094-853
Product ID 68094-853_7670a1a9-f14e-4e9e-8b3e-f8d5e52125e0
Description

10 BLISTER PACK in 1 CARTON (68094-853-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)

Marketing

Marketing Status
Marketed Since 2024-08-15
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": "7670a1a9-f14e-4e9e-8b3e-f8d5e52125e0", "openfda": {"upc": ["0368094853620"], "unii": ["Z6375YW9SF"], "rxcui": ["1483744"], "spl_set_id": ["74087d2f-468d-4de1-a2fc-a489d0f2abef"], "manufacturer_name": ["Precision Dose Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68094-853-61)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)", "package_ndc": "68094-853-61", "marketing_start_date": "20240815"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68094-853-62)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)", "package_ndc": "68094-853-62", "marketing_end_date": "20261231", "marketing_start_date": "20141029"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68094-853-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)", "package_ndc": "68094-853-66", "marketing_start_date": "20240815"}], "brand_name": "Naltrexone Hydrochloride", "product_id": "68094-853_7670a1a9-f14e-4e9e-8b3e-f8d5e52125e0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "68094-853", "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_start_date": "20141029", "listing_expiration_date": "20261231"}