Package 36000-308-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 36000-308-10
Digits Only 3600030810
Product NDC 36000-308
Product ID 36000-308_ad8223dd-206d-4fd8-b0fb-de10e970a9e1
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (36000-308-10) / 1 mL in 1 VIAL, SINGLE-DOSE (36000-308-01)

Marketing

Marketing Status
Marketed Since 2021-01-29
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": "ad8223dd-206d-4fd8-b0fb-de10e970a9e1", "openfda": {"upc": ["0336000308014"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["d04ae2d7-01b9-405d-bb7a-bf2d876ce26a"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (36000-308-10)  / 1 mL in 1 VIAL, SINGLE-DOSE (36000-308-01)", "package_ndc": "36000-308-10", "marketing_start_date": "20210129"}], "brand_name": "naloxone hydrochloride", "product_id": "36000-308_ad8223dd-206d-4fd8-b0fb-de10e970a9e1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "36000-308", "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": "ANDA214785", "marketing_category": "ANDA", "marketing_start_date": "20210129", "listing_expiration_date": "20271231"}