Package 76329-3469-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76329-3469-1
Digits Only 7632934691
Product NDC 76329-3469
Product ID 76329-3469_2ab20a74-a067-4d43-84fb-fe331192c34b
Description

10 SYRINGE in 1 BOX (76329-3469-1) / 2 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2016-07-28
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": ["PARENTERAL"], "spl_id": "2ab20a74-a067-4d43-84fb-fe331192c34b", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["d2f5bfa0-933e-46d0-8b1a-9f90e6aaba54"], "manufacturer_name": ["International Medication Systems, Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 BOX (76329-3469-1)  / 2 mL in 1 SYRINGE", "package_ndc": "76329-3469-1", "marketing_start_date": "20160728"}], "brand_name": "Naloxone Hydrochloride", "product_id": "76329-3469_2ab20a74-a067-4d43-84fb-fe331192c34b", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "76329-3469", "generic_name": "Naloxone Hydrochloride", "labeler_name": "International Medication Systems, Limited", "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": "20160728", "listing_expiration_date": "20261231"}