NDC 72078-034 – Ultiva

Remifentanil Hydrochloride 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug DEA schedule CII

Product NDC72078-034

Product details

Brand name
Ultiva
Generic name
Remifentanil Hydrochloride
Labeler
Mylan Institutional LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA020630
Marketed since
June 21, 2023
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ultiva →

Package NDC codes (1)

Package NDCDescriptionSince
72078-034-0110 VIAL, GLASS in 1 CARTON (72078-034-01) / 3 mL in 1 VIAL, GLASS (72078-034-00)Jun 21, 2023

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