Package 42023-114-10

Brand: ketalar

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42023-114-10
Digits Only 4202311410
Product NDC 42023-114
Product ID 42023-114_0f521490-2803-43cd-baf9-e0ab303694d0
Description

10 VIAL in 1 CARTON (42023-114-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2007-10-01
Brand ketalar
Generic ketamine hydrochloride
Sample Package No

Linked Drug Pages (1)

Ketalar ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0f521490-2803-43cd-baf9-e0ab303694d0", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["206967", "206970", "206972", "238082", "238083", "238084"], "spl_set_id": ["14e8f864-8b8a-4e7e-8439-e510d3107063"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (42023-114-10)  / 10 mL in 1 VIAL", "package_ndc": "42023-114-10", "marketing_start_date": "20071001"}], "brand_name": "Ketalar", "product_id": "42023-114_0f521490-2803-43cd-baf9-e0ab303694d0", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "42023-114", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketalar", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "NDA016812", "marketing_category": "NDA", "marketing_start_date": "20071001", "listing_expiration_date": "20261231"}