Package 67457-912-01
Brand: ultiva
Generic: remifentanil hydrochloridePackage Facts
Identity
Package NDC
67457-912-01
Digits Only
6745791201
Product NDC
67457-912
Description
10 VIAL, GLASS in 1 CARTON (67457-912-01) / 3 mL in 1 VIAL, GLASS (67457-912-00)
Marketing
Marketing Status
Brand
ultiva
Generic
remifentanil hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4e4a5266-148c-4137-8fed-74766f8c1c7e", "openfda": {"unii": ["5V444H5WIC"], "rxcui": ["1729578", "1729581", "1729584", "1729586", "1729710", "1729712"], "spl_set_id": ["4dbcb8f9-1987-4b66-bd2f-d251fda0be10"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (67457-912-01) / 3 mL in 1 VIAL, GLASS (67457-912-00)", "package_ndc": "67457-912-01", "marketing_start_date": "20200415"}], "brand_name": "Ultiva", "product_id": "67457-912_4e4a5266-148c-4137-8fed-74766f8c1c7e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67457-912", "dea_schedule": "CII", "generic_name": "Remifentanil Hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ultiva", "active_ingredients": [{"name": "REMIFENTANIL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "NDA020630", "marketing_category": "NDA", "marketing_start_date": "20200415", "listing_expiration_date": "20261231"}