Package 68083-504-10
Brand: ketamine hydrochloride
Generic: ketamine hydrochloridePackage Facts
Identity
Package NDC
68083-504-10
Digits Only
6808350410
Product NDC
68083-504
Description
10 VIAL in 1 CARTON (68083-504-10) / 20 mL in 1 VIAL
Marketing
Marketing Status
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": "5a07aea6-9e9a-4788-9a14-e624b4f86bc0", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238082", "238083", "238084"], "spl_set_id": ["b96a0a23-3ca0-4a92-bd8b-1e9921931772"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (68083-504-10) / 20 mL in 1 VIAL", "package_ndc": "68083-504-10", "marketing_start_date": "20230124"}], "brand_name": "Ketamine Hydrochloride", "product_id": "68083-504_5a07aea6-9e9a-4788-9a14-e624b4f86bc0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "68083-504", "dea_schedule": "CIII", "generic_name": "Ketamine Hydrochloride", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketamine Hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216809", "marketing_category": "ANDA", "marketing_start_date": "20230124", "listing_expiration_date": "20261231"}