NDC Package 22840-0301-2 Short And Giant Ragweed Pollen Mix

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
22840-0301-2
Package Description:
10 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Short And Giant Ragweed Pollen Mix
Usage Information:
INDICATIONSHyposensitization is indicated when careful testing and patient history can pinpoint allergens responsible for allergic symptoms, and when it is not possible or practical to avoid these allergens. Allergenic extracts are administered to reduce symptoms of allergy of a seasonal or perennial nature.
11-Digit NDC Billing Format:
22840030102
NDC to RxNorm Crosswalk:
  • RxCUI: 896138 - short ragweed pollen extract 50 MG/ML Injectable Solution
  • RxCUI: 896138 - Ambrosia artemisiifolia pollen extract 0.05 GM/ML Injectable Solution
  • RxCUI: 896138 - Ambrosia artemisiifolia pollen extract 50 MG/ML Injectable Solution
  • RxCUI: 899534 - giant ragweed pollen extract 25 MG/ML / short ragweed pollen extract 25 MG/ML Injectable Solution
  • RxCUI: 899534 - giant ragweed pollen extract 25 MG/ML / western ragweed pollen extract 25 MG/ML Injectable Solution
  • Labeler Name:
    Greer Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    09-15-1981
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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
    22840-0301-450 mL in 1 VIAL, MULTI-DOSE
    22840-0301-55 mL in 1 BOTTLE, DROPPER

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 22840-0301-2?

    The NDC Packaged Code 22840-0301-2 is assigned to a package of 10 ml in 1 vial, multi-dose of Short And Giant Ragweed Pollen Mix, labeled by Greer Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 22840-0301 included in the NDC Directory?

    No, Short And Giant Ragweed Pollen Mix with product code 22840-0301 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Greer Laboratories, Inc. on September 15, 1981 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 22840-0301-2?

    The 11-digit format is 22840030102. 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 5-4-1 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
    5-4-122840-0301-25-4-222840-0301-02