1. Home
  2. Labeler Index
  3. Sanofi Pasteur Inc.
  4. 49281-912
  5. NDC Package Code: 49281-912-10 Diluent

NDC Package 49281-912-10 Diluent

Sodium Chloride Injection Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
49281-912-10
Package Description:
1 VIAL, MULTI-DOSE in 1 PACKAGE / 3 mL in 1 VIAL, MULTI-DOSE (49281-912-69)
Product Code:
49281-912
Proprietary Name:
Diluent
Non-Proprietary Name:
Sodium Chloride
Substance Name:
Sodium Chloride
Usage Information:
This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
11-Digit NDC Billing Format:
49281091210
NDC to RxNorm Crosswalk:
  • RxCUI: 1292826 - yellow fever vaccine (generic for YF-Vax) Injectable Suspension
  • RxCUI: 1292826 - yellow fever virus strain 17D-204 live antigen 4000 UNT/ML Injectable Suspension
  • RxCUI: 1292828 - YF-VAX Injectable Suspension
  • RxCUI: 1292828 - yellow fever virus strain 17D-204 live antigen 4000 UNT/ML Injectable Suspension [YF-Vax]
  • RxCUI: 1292828 - YF-Vax 4000 UNT/ML Injectable Suspension
    • Product Type:
    Vaccine
    Labeler Name:
    Sanofi Pasteur Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • SODIUM CHLORIDE 4.5 mg/.5mL
    • Pharmacologic Class(es):
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    BLA103915
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    05-22-1953
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    49281-912-055 VIAL, SINGLE-DOSE in 1 PACKAGE / .6 mL in 1 VIAL, SINGLE-DOSE (49281-912-59)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49281-912-10?

    The NDC Packaged Code 49281-912-10 is assigned to a package of 1 vial, multi-dose in 1 package / 3 ml in 1 vial, multi-dose (49281-912-69) of Diluent, a vaccine label labeled by Sanofi Pasteur Inc.. The product's dosage form is injection and is administered via subcutaneous form.

    Is NDC 49281-912 included in the NDC Directory?

    Yes, Diluent with product code 49281-912 is active and included in the NDC Directory. The product was first marketed by Sanofi Pasteur Inc. on May 22, 1953 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49281-912-10?

    The 11-digit format is 49281091210. 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
    5-3-249281-912-105-4-249281-0912-10