Package 25021-682-20

Brand: ketamine hydrochloride

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-682-20
Digits Only 2502168220
Product NDC 25021-682
Product ID 25021-682_51a16c65-47e0-405c-8c84-82a6a28b3efd
Description

10 VIAL in 1 CARTON (25021-682-20) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-07-15
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": "51a16c65-47e0-405c-8c84-82a6a28b3efd", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["238082", "238083", "238084"], "spl_set_id": ["902c3785-a3cb-472b-ac15-394ac646271d"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-682-20)  / 20 mL in 1 VIAL", "package_ndc": "25021-682-20", "marketing_start_date": "20230715"}], "brand_name": "Ketamine Hydrochloride", "product_id": "25021-682_51a16c65-47e0-405c-8c84-82a6a28b3efd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "25021-682", "dea_schedule": "CIII", "generic_name": "Ketamine Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ketamine Hydrochloride", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216809", "marketing_category": "ANDA", "marketing_start_date": "20230715", "listing_expiration_date": "20261231"}