NDC Package 49643-010-30 Flaxseed

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:
49643-010-30
Package Description:
30 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Flaxseed
Usage Information:
Allergenic extract may be used as a diagnostic skin test reagent in persons suspected of being sensitive to the allergenic source material from which the extract is made. Skin tests should be used in conjunction with a thorough allergic history to establish the relevance of a given allergen in the etiology of allergic disease. 4,5,6 Immunotherapy with allergenic extract is indicated in persons suffering from allergic rhinitis, bronchitis, conjunctivitis, urticaria and asthma. The therapeutic efficacy of allergenic extract has been proven in ragweed, grass, and mountain cedar pollinosis, cat-induced asthma and hypersensitivity to hymenoptera venoms. 7-12 Immunotherapy may be used along with or exclusive of antihistamines and other medications used to control allergic symptoms.
11-Digit NDC Billing Format:
49643001030
NDC to RxNorm Crosswalk:
  • RxCUI: 1011991 - Trichothecium roseum allergenic extract 100 MG/mL Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum allergenic extract 100 MG/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 0.1 GM/ML Injectable Solution
  • RxCUI: 1011991 - Trichothecium roseum extract 100 MG/ML Injectable Solution
  • RxCUI: 1115265 - bluegum eucalyptus pollen extract 50 MG/ML Injectable Solution
  • Labeler Name:
    Allermed Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    03-12-1974
    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
    49643-010-055 mL in 1 VIAL, MULTI-DOSE
    49643-010-1010 mL in 1 VIAL, MULTI-DOSE
    49643-010-5050 mL in 1 VIAL, MULTI-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49643-010-30?

    The NDC Packaged Code 49643-010-30 is assigned to a package of 30 ml in 1 vial, multi-dose of Flaxseed, labeled by Allermed Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 49643-010 included in the NDC Directory?

    No, Flaxseed with product code 49643-010 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 12, 1974 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 49643-010-30?

    The 11-digit format is 49643001030. 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
    5-3-249643-010-305-4-249643-0010-30