Package 72572-450-25

Brand: naloxone hydrochloride

Generic: nalxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72572-450-25
Digits Only 7257245025
Product NDC 72572-450
Product ID 72572-450_9d4007b7-f036-40c2-bbbe-0176fc62f249
Description

25 VIAL in 1 CARTON (72572-450-25) / 1 mL in 1 VIAL (72572-450-01)

Marketing

Marketing Status
Marketed Since 2019-11-11
Brand naloxone hydrochloride
Generic nalxone 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": "9d4007b7-f036-40c2-bbbe-0176fc62f249", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["21d20dff-6efe-481e-a5a0-9c80ded73ca9"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-450-25)  / 1 mL in 1 VIAL (72572-450-01)", "package_ndc": "72572-450-25", "marketing_start_date": "20191111"}], "brand_name": "Naloxone Hydrochloride", "product_id": "72572-450_9d4007b7-f036-40c2-bbbe-0176fc62f249", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "72572-450", "generic_name": "Nalxone Hydrochloride", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA070299", "marketing_category": "ANDA", "marketing_start_date": "20191111", "listing_expiration_date": "20261231"}