Package 71205-707-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-707-02
Digits Only 7120570702
Product NDC 71205-707
Product ID 71205-707_8d529b4c-85fd-4e50-9443-9080825307bf
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (71205-707-02) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-10-20
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": "8d529b4c-85fd-4e50-9443-9080825307bf", "openfda": {"upc": ["0371205707026"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["8d529b4c-85fd-4e50-9443-9080825307bf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (71205-707-02)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71205-707-02", "marketing_start_date": "20221020"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "71205-707_8d529b4c-85fd-4e50-9443-9080825307bf", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71205-707", "generic_name": "naloxone hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20220621", "listing_expiration_date": "20261231"}