NDC Package 49643-315-50 Short Ragweed

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:
49643-315-50
Package Description:
50 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Short Ragweed
Usage Information:
Studies have shown that properly performed an interpreted skin tests with ragweed pollen extract are useful in the diagnosis of allergy to ragweed pollen 7, 8, 20, 21. Immunotherapy with the appropriate dosage of short ragweed pollen extract is effective in reducing symptoms of hay fever and asthma resulting from exposure to short ragweed pollen (9, 10, 11), and it is believed to be effective with extract of giant ragweed, although carefully controlled studies are unavailable. However, clinical observations and known cross reactivity between short and giant ragweed pollens have led to the practice of using a mixture of the two species for skin testing and treatment 22, 23, 24, 25, 26, 27. This form of treatment is recommended for patients who cannot avoid exposure to pollen and who do not obtain satisfactory relief of symptoms from other medications, such as antihistamines. Immunologic changes resulting from treatment with short ragweed pollen extract are believed to include: The induction of specific anti-ragweed IgG antibodies commonly referred to as "blocking antibodies" 12, 13. A decrease in the elevation of ragweed specific IgE during and immediately following the ragweed pollen season 14. A reduction of circulating anti-ragweed IgE after long-term immunotherapy 15. A decrease in skin reactivity to the extract 16 and a decrease in leukocyte sensitivity to histamine release 17 after long-term immunotherapy.
11-Digit NDC Billing Format:
49643031550
NDC to RxNorm Crosswalk:
  • RxCUI: 896140 - short ragweed pollen extract 100 MG/ML Injectable Solution
  • RxCUI: 896140 - Ambrosia artemisiifolia pollen extract 1 GM per 10 ML Injectable Solution
  • RxCUI: 896140 - Ambrosia artemisiifolia pollen extract 100 MG/ML Injectable Solution
  • Labeler Name:
    Allermed Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    03-22-1982
    Listing Expiration Date:
    12-31-2022
    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
    49643-315-055 mL in 1 VIAL, MULTI-DOSE
    49643-315-1010 mL in 1 VIAL, MULTI-DOSE
    49643-315-3030 mL in 1 VIAL, MULTI-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49643-315-50?

    The NDC Packaged Code 49643-315-50 is assigned to a package of 50 ml in 1 vial, multi-dose of Short Ragweed, labeled by Allermed Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 49643-315 included in the NDC Directory?

    No, Short Ragweed with product code 49643-315 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Allermed Laboratories, Inc. on March 22, 1982 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49643-315-50?

    The 11-digit format is 49643031550. 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
    5-3-249643-315-505-4-249643-0315-50