Package 72078-036-05

Brand: ultiva

Generic: remifentanil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72078-036-05
Digits Only 7207803605
Product NDC 72078-036
Description

10 VIAL, GLASS in 1 CARTON (72078-036-05) / 10 mL in 1 VIAL, GLASS (72078-036-00)

Marketing

Marketing Status
Marketed Since 2024-12-16
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 (72078-036-05)  / 10 mL in 1 VIAL, GLASS (72078-036-00)", "package_ndc": "72078-036-05", "marketing_start_date": "20241216"}], "brand_name": "Ultiva", "product_id": "72078-036_594087a1-25f2-4f68-aea6-ad7df40559ab", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72078-036", "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": "20241216", "listing_expiration_date": "20261231"}