NDC Package 10019-655-06 Sevoflurane

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:
10019-655-06
Package Description:
6 BOTTLE in 1 CARTON / 250 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Sevoflurane
Non-Proprietary Name:
Sevoflurane
Substance Name:
Sevoflurane
Usage Information:
Sevoflurane, USP is indicated for induction and maintenance of general anesthesia in adult and pediatric patients for inpatient and outpatient surgery.Sevoflurane, USP should be administered only by persons trained in the administration of general anesthesia. Facilities for maintenance of a patent airway, artificial ventilation, oxygen enrichment, and circulatory resuscitation must be immediately available. Since level of anesthesia may be altered rapidly, only vaporizers producing predictable concentrations of sevoflurane, USP should be used.
11-Digit NDC Billing Format:
10019065506
NDC to RxNorm Crosswalk:
  • RxCUI: 200243 - sevoflurane 100 % Inhalation Solution
  • RxCUI: 200243 - sevoflurane 1000 MG/ML Inhalation Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Baxter Healthcare Corporation
    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:
    ANDA075895
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-02-2002
    Listing Expiration Date:
    12-31-2025
    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 10019-655-06?

    The NDC Packaged Code 10019-655-06 is assigned to a package of 6 bottle in 1 carton / 250 ml in 1 bottle of Sevoflurane, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is liquid and is administered via respiratory (inhalation) form.

    Is NDC 10019-655 included in the NDC Directory?

    Yes, Sevoflurane with product code 10019-655 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on July 02, 2002 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10019-655-06?

    The 11-digit format is 10019065506. 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
    5-3-210019-655-065-4-210019-0655-06