Package 72603-590-25

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-590-25
Digits Only 7260359025
Product NDC 72603-590
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72603-590-01)

Marketing

Marketing Status
Marketed Since 2024-07-01
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": "3fb9f554-709f-4f32-96fc-60cb4b867ae5", "openfda": {"upc": ["0372603590012", "0372603590104"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["d4c44b74-4e36-4b63-80eb-64ce99ccb39f"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-10)  / 1 mL in 1 VIAL, SINGLE-DOSE (72603-590-01)", "package_ndc": "72603-590-10", "marketing_start_date": "20240701"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (72603-590-01)", "package_ndc": "72603-590-25", "marketing_start_date": "20240701"}], "brand_name": "naloxone hydrochloride", "product_id": "72603-590_3fb9f554-709f-4f32-96fc-60cb4b867ae5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "72603-590", "generic_name": "naloxone hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "naloxone hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA218404", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}