Package 65219-186-23

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65219-186-23
Digits Only 6521918623
Product NDC 65219-186
Product ID 65219-186_cc4da24f-92ef-40c9-a77d-afa3164bb5b8
Description

10 VIAL in 1 TRAY (65219-186-23) / 5 mL in 1 VIAL (65219-186-13)

Marketing

Marketing Status
Marketed Since 2025-04-18
Brand ketamine hydrochloride
Generic ketamine hydrochloride
Sample Package No

Linked Drug Pages (1)

ketamine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "cc4da24f-92ef-40c9-a77d-afa3164bb5b8", "openfda": {"upc": ["0365219186137"], "unii": ["O18YUO0I83"], "rxcui": ["238083"], "spl_set_id": ["ac2e715d-251c-4e3f-b91c-972f466d0beb"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (65219-186-23)  / 5 mL in 1 VIAL (65219-186-13)", "package_ndc": "65219-186-23", "marketing_start_date": "20250418"}], "brand_name": "ketamine hydrochloride", "product_id": "65219-186_cc4da24f-92ef-40c9-a77d-afa3164bb5b8", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "65219-186", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ketamine hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA215808", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}