Package 46122-812-71

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 46122-812-71
Digits Only 4612281271
Product NDC 46122-812
Product ID 46122-812_7232f412-39b6-47d5-8f9a-0c1559435a3f
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (46122-812-71) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-03-12
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": "7232f412-39b6-47d5-8f9a-0c1559435a3f", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["cce38c13-0d2f-49bb-94fa-6f2bbb4d5984"], "manufacturer_name": ["AMERISOURCE BERGEN"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (46122-812-71)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "46122-812-71", "marketing_start_date": "20250312"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "46122-812_7232f412-39b6-47d5-8f9a-0c1559435a3f", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "46122-812", "generic_name": "naloxone hydrochloride", "labeler_name": "AMERISOURCE BERGEN", "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": "20250312", "listing_expiration_date": "20261231"}