Package 0409-0040-10

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-0040-10
Digits Only 0409004010
Product NDC 0409-0040
Product ID 0409-0040_aa1e5788-73a9-4b95-99da-17eb252f8702
Description

10 VIAL, MULTI-DOSE in 1 CARTON (0409-0040-10) / 5 mL in 1 VIAL, MULTI-DOSE (0409-0040-05)

Marketing

Marketing Status
Marketed Since 2022-10-10
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": "aa1e5788-73a9-4b95-99da-17eb252f8702", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238083"], "spl_set_id": ["390f2db8-0fcd-4648-b584-9effa084be27"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0409-0040-10)  / 5 mL in 1 VIAL, MULTI-DOSE (0409-0040-05)", "package_ndc": "0409-0040-10", "marketing_start_date": "20221010"}], "brand_name": "Ketamine Hydrochloride", "product_id": "0409-0040_aa1e5788-73a9-4b95-99da-17eb252f8702", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0409-0040", "dea_schedule": "CIII", "generic_name": "KETAMINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketamine Hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA074549", "marketing_category": "ANDA", "marketing_start_date": "20221010", "listing_expiration_date": "20261231"}