Package 0404-9922-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9922-02
Digits Only 0404992202
Product NDC 0404-9922
Product ID 0404-9922_ace20fdd-3422-48d9-acf4-da37f78f13a7
Description

1 SYRINGE in 1 BAG (0404-9922-02) / 2 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2022-01-13
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": ["PARENTERAL"], "spl_id": "ace20fdd-3422-48d9-acf4-da37f78f13a7", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["bd65e3fe-cd7a-4855-8f55-8cc3a0921ccc"], "manufacturer_name": ["Henry Schein, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (0404-9922-02)  / 2 mL in 1 SYRINGE", "package_ndc": "0404-9922-02", "marketing_start_date": "20220113"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9922_ace20fdd-3422-48d9-acf4-da37f78f13a7", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9922", "generic_name": "naloxone hydrochloride", "labeler_name": "Henry Schein, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA072076", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20271231"}