Package 0093-2165-68

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-2165-68
Digits Only 0093216568
Product NDC 0093-2165
Product ID 0093-2165_f68e5624-94f3-4331-8db9-5affce1fb2f7
Description

2 BLISTER PACK in 1 CARTON (0093-2165-68) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0093-2165-19) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Discontinued 2026-06-30
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "f68e5624-94f3-4331-8db9-5affce1fb2f7", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["4a72d8cf-3c24-47d8-94d1-4e175f2da264"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0093-2165-68)  / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0093-2165-19)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0093-2165-68", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0093-2165_f68e5624-94f3-4331-8db9-5affce1fb2f7", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0093-2165", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA209522", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20211222"}