Package 70518-2725-0

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2725-0
Digits Only 7051827250
Product NDC 70518-2725
Product ID 70518-2725_4a7f0729-7531-bba3-e063-6294a90a001b
Description

10 SYRINGE in 1 BOX (70518-2725-0) / 2 mL in 1 SYRINGE (70518-2725-1)

Marketing

Marketing Status
Marketed Since 2020-05-05
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["PARENTERAL"], "spl_id": "4a7f0729-7531-bba3-e063-6294a90a001b", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["68df290c-d776-4cfc-9565-332eb56c4723"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 BOX (70518-2725-0)  / 2 mL in 1 SYRINGE (70518-2725-1)", "package_ndc": "70518-2725-0", "marketing_start_date": "20200505"}], "brand_name": "Naloxone Hydrochloride", "product_id": "70518-2725_4a7f0729-7531-bba3-e063-6294a90a001b", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70518-2725", "generic_name": "Naloxone Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20200505", "listing_expiration_date": "20271231"}