Package 0143-9509-10

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9509-10
Digits Only 0143950910
Product NDC 0143-9509
Product ID 0143-9509_6ada9356-0968-46df-b067-d95509650c48
Description

10 VIAL in 1 BOX (0143-9509-10) / 5 mL in 1 VIAL (0143-9509-01)

Marketing

Marketing Status
Marketed Since 1996-07-01
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": "6ada9356-0968-46df-b067-d95509650c48", "openfda": {"upc": ["0301439508106", "0301439509103"], "unii": ["O18YUO0I83"], "rxcui": ["238083", "238084"], "spl_set_id": ["58487c78-a641-4278-acc0-343596ee8683"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (0143-9509-10)  / 5 mL in 1 VIAL (0143-9509-01)", "package_ndc": "0143-9509-10", "marketing_start_date": "19960701"}], "brand_name": "Ketamine Hydrochloride", "product_id": "0143-9509_6ada9356-0968-46df-b067-d95509650c48", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0143-9509", "dea_schedule": "CIII", "generic_name": "Ketamine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA 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": "19960701", "listing_expiration_date": "20261231"}