Package 68001-645-45

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-645-45
Digits Only 6800164545
Product NDC 68001-645
Product ID 68001-645_402a0c78-5e4d-39a0-e063-6294a90a74ee
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (68001-645-45) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-05-01
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": "402a0c78-5e4d-39a0-e063-6294a90a74ee", "openfda": {"upc": ["0368001645454"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["327004b0-560a-84d0-e063-6294a90aa743"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (68001-645-45)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-645-45", "marketing_start_date": "20250501"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "68001-645_402a0c78-5e4d-39a0-e063-6294a90a74ee", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "68001-645", "generic_name": "naloxone hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}