Package 55150-439-10

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-439-10
Digits Only 5515043910
Product NDC 55150-439
Product ID 55150-439_35913e3d-e141-4596-bc4c-72deb8cbf932
Description

10 VIAL, MULTI-DOSE in 1 CARTON (55150-439-10) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2021-03-15
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": "35913e3d-e141-4596-bc4c-72deb8cbf932", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238082", "238083", "238084"], "spl_set_id": ["f8b01c77-620d-4734-a771-b8524b65bcca"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (55150-439-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-439-10", "marketing_start_date": "20210315"}], "brand_name": "KETAMINE HYDROCHLORIDE", "product_id": "55150-439_35913e3d-e141-4596-bc4c-72deb8cbf932", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "55150-439", "dea_schedule": "CIII", "generic_name": "KETAMINE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA076092", "marketing_category": "ANDA", "marketing_start_date": "20210315", "listing_expiration_date": "20261231"}