Package 72078-034-01
Brand: ultiva
Generic: remifentanil hydrochloridePackage Facts
Identity
Package NDC
72078-034-01
Digits Only
7207803401
Product NDC
72078-034
Description
10 VIAL, GLASS in 1 CARTON (72078-034-01) / 3 mL in 1 VIAL, GLASS (72078-034-00)
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": "594087a1-25f2-4f68-aea6-ad7df40559ab", "openfda": {"unii": ["5V444H5WIC"], "rxcui": ["1729578", "1729581", "1729584", "1729586", "1729710", "1729712"], "spl_set_id": ["8b4c8696-e23e-4c51-a4d2-babab5bd945a"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (72078-034-01) / 3 mL in 1 VIAL, GLASS (72078-034-00)", "package_ndc": "72078-034-01", "marketing_start_date": "20230621"}], "brand_name": "Ultiva", "product_id": "72078-034_594087a1-25f2-4f68-aea6-ad7df40559ab", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72078-034", "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": "20230621", "listing_expiration_date": "20261231"}