Package 0404-9882-10

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9882-10
Digits Only 0404988210
Product NDC 0404-9882
Product ID 0404-9882_fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9
Description

1 VIAL in 1 BAG (0404-9882-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-11
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": "fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238084"], "spl_set_id": ["dd8eff00-b92e-4f48-8b57-0464484d6ddf"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9882-10)  / 10 mL in 1 VIAL", "package_ndc": "0404-9882-10", "marketing_start_date": "20220111"}], "brand_name": "KETAMINE HYDROCHLORIDE", "product_id": "0404-9882_fb0436cf-9ef7-4b0b-8c47-8068ffc0bbf9", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0404-9882", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA074549", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}