NDC Package 52584-641-64 Suprane

Desflurane Liquid Respiratory (inhalation) - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
52584-641-64
Package Description:
1 BOTTLE in 1 BAG / 240 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Suprane
Non-Proprietary Name:
Desflurane
Substance Name:
Desflurane
Usage Information:
The use of SUPRANE is contraindicated in the following conditions:Known or suspected genetic susceptibility to malignant hyperthermia.Patients in whom general anesthesia is contraindicated.Patients with known sensitivity to SUPRANEĀ or to other halogenated agents [see Warnings and Precautions (5.5)].Patients with a history of moderate to severe hepatic dysfunction following anesthesia with SUPRANE or other halogenated agents and not otherwise explained [see Warnings and Precautions (5.5)].
11-Digit NDC Billing Format:
52584064164
NDC to RxNorm Crosswalk:
  • RxCUI: 208919 - Suprane 100 % Inhalation Solution
  • RxCUI: 208919 - desflurane 1000 MG/ML Inhalation Solution [Suprane]
  • RxCUI: 208919 - Suprane 1 ML/ML Inhalation Solution
  • RxCUI: 562366 - desflurane 100 % Inhalation Solution
  • RxCUI: 562366 - desflurane 1000 MG/ML Inhalation Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    General Injectables & Vaccines, Inc
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA020118
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-25-2012
    End Marketing Date:
    01-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52584-641-64?

    The NDC Packaged Code 52584-641-64 is assigned to a package of 1 bottle in 1 bag / 240 ml in 1 bottle of Suprane, a human prescription drug labeled by General Injectables & Vaccines, Inc. The product's dosage form is liquid and is administered via respiratory (inhalation) form.

    Is NDC 52584-641 included in the NDC Directory?

    Yes, Suprane with product code 52584-641 is active and included in the NDC Directory. The product was first marketed by General Injectables & Vaccines, Inc on April 25, 2012.

    What is the 11-digit format for NDC 52584-641-64?

    The 11-digit format is 52584064164. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-252584-641-645-4-252584-0641-64