Package 72572-321-10

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72572-321-10
Digits Only 7257232110
Product NDC 72572-321
Description

10 VIAL in 1 BOX (72572-321-10) / 5 mL in 1 VIAL (72572-321-01)

Marketing

Marketing Status
Marketed Since 2019-12-05
Brand ketamine hydrochloride
Generic ketamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "675b63de-32c3-4205-9532-f018e3d3761a", "openfda": {"upc": ["0372572321105"], "unii": ["O18YUO0I83"], "rxcui": ["238083", "238084"], "spl_set_id": ["58c86d9b-8694-4bd8-8254-f19ee3ad60b0"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (72572-321-10)  / 5 mL in 1 VIAL (72572-321-01)", "package_ndc": "72572-321-10", "marketing_start_date": "20191205"}], "brand_name": "Ketamine Hydrochloride", "product_id": "72572-321_675b63de-32c3-4205-9532-f018e3d3761a", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "72572-321", "dea_schedule": "CIII", "generic_name": "Ketamine Hydrochloride", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketamine Hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA074524", "marketing_category": "ANDA", "marketing_start_date": "20191205", "listing_expiration_date": "20261231"}