Package 0363-2140-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-2140-02
Digits Only 0363214002
Product NDC 0363-2140
Product ID 0363-2140_9ae58c12-1542-4a7f-82a2-6e0c989615bd
Description

2 VIAL in 1 CARTON (0363-2140-02) / .1 mL in 1 VIAL (0363-2140-01)

Marketing

Marketing Status
Marketed Since 2024-04-24
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": "9ae58c12-1542-4a7f-82a2-6e0c989615bd", "openfda": {"upc": ["0311917040332"], "unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["3829826b-e48f-4e26-869f-6b9e4ee0a840"], "manufacturer_name": ["Walgreen Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL in 1 CARTON (0363-2140-02)  / .1 mL in 1 VIAL (0363-2140-01)", "package_ndc": "0363-2140-02", "marketing_start_date": "20240424"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0363-2140_9ae58c12-1542-4a7f-82a2-6e0c989615bd", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0363-2140", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Walgreen Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA217992", "marketing_category": "ANDA", "marketing_start_date": "20240424", "listing_expiration_date": "20271231"}