ULTIVA® Remifentanil HCl

NDC: 67457-0198-03, 72078-0034-01, 67457-0198-05, 72078-0035-02

This product is a DEA Schedule II controlled substance. A DEA Form 222, valid state and federal licensing, and a completed and current “Know Your Customer” questionnaire are required. Additional order restrictions will apply.

Product specifications

SKU:
ULTI-main
Schedule Classification:
Class 2
Dosage Form:
Single-Dose Vial
Quantity Packaging:
10/BX