Package 71872-7297-1
Brand: naloxone hydrochloride
Generic: naloxone hydrochloridePackage Facts
Identity
Package NDC
71872-7297-1
Digits Only
7187272971
Product NDC
71872-7297
Description
1 VIAL, SINGLE-DOSE in 1 BAG (71872-7297-1) / 1 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
naloxone hydrochloride
Generic
naloxone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "fa1ca55b-f56c-0d9b-e053-6294a90a258a", "openfda": {"upc": ["0336000308014"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["fa1ca55b-f56b-0d9b-e053-6294a90a258a"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7297-1) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7297-1", "marketing_start_date": "20221116"}], "brand_name": "naloxone hydrochloride", "product_id": "71872-7297_fa1ca55b-f56c-0d9b-e053-6294a90a258a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7297", "generic_name": "naloxone hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "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": "20261231"}