Package 0404-9880-20

Brand: ketalar

Generic: ketamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9880-20
Digits Only 0404988020
Product NDC 0404-9880
Product ID 0404-9880_66dc4477-9189-4ff8-b778-8ceb17a50802
Description

1 VIAL in 1 BAG (0404-9880-20) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-11
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": "66dc4477-9189-4ff8-b778-8ceb17a50802", "openfda": {"unii": ["O18YUO0I83"], "rxcui": ["206967", "238082"], "spl_set_id": ["46dab560-8ecd-4d92-8c92-6baa2310b09b"], "manufacturer_name": ["Henry Schein, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9880-20)  / 20 mL in 1 VIAL", "package_ndc": "0404-9880-20", "marketing_start_date": "20220111"}], "brand_name": "KETALAR", "product_id": "0404-9880_66dc4477-9189-4ff8-b778-8ceb17a50802", "dosage_form": "INJECTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "0404-9880", "dea_schedule": "CIII", "generic_name": "ketamine hydrochloride", "labeler_name": "Henry Schein, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KETALAR", "active_ingredients": [{"name": "KETAMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "NDA016812", "marketing_category": "NDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}