Package 36000-310-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 36000-310-02
Digits Only 3600031002
Product NDC 36000-310
Product ID 36000-310_bde02e6f-da64-4b2b-80f2-2c0ab9783483
Description

1 VIAL, MULTI-DOSE in 1 CARTON (36000-310-02) / 10 mL in 1 VIAL, MULTI-DOSE (36000-310-01)

Marketing

Marketing Status
Marketed Since 2022-11-07
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": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "bde02e6f-da64-4b2b-80f2-2c0ab9783483", "openfda": {"upc": ["0336000310017"], "unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["3d8813be-6d22-46f1-ac25-0d8a817a521c"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (36000-310-02)  / 10 mL in 1 VIAL, MULTI-DOSE (36000-310-01)", "package_ndc": "36000-310-02", "marketing_start_date": "20221107"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "36000-310_bde02e6f-da64-4b2b-80f2-2c0ab9783483", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "36000-310", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA214792", "marketing_category": "ANDA", "marketing_start_date": "20221107", "listing_expiration_date": "20261231"}