NDC Package 36987-1314-4 Cranberry

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:
36987-1314-4
Package Description:
50 mL in 1 VIAL, MULTI-DOSE
Product Code:
Proprietary Name:
Cranberry
Usage Information:
Cranberry has been used for reducing the risk of "bladder infections" (urinary tract infections). It has also been used for decreasing the smell of urine in people who are unable to control urination (incontinent). This product should not be used alone to treat bladder infections. It may not work, and the delay could allow the infection to worsen. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
11-Digit NDC Billing Format:
36987131404
NDC to RxNorm Crosswalk:
  • RxCUI: 1000013 - whole wheat allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1000013 - whole wheat allergenic extract 0.05 GM/ML Injectable Solution
  • RxCUI: 1000013 - whole wheat extract 50 MG/ML Injectable Solution
  • RxCUI: 1006513 - barley malt allergenic extract 50 MG/ML Injectable Solution
  • RxCUI: 1006513 - barley (malt) allergenic extract 0.05 GM/ML Injectable Solution
  • Labeler Name:
    Nelco Laboratories, Inc.
    Sample Package:
    No
    Start Marketing Date:
    08-29-1972
    Listing Expiration Date:
    12-31-2017
    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
    36987-1314-15 mL in 1 VIAL, MULTI-DOSE
    36987-1314-210 mL in 1 VIAL, MULTI-DOSE
    36987-1314-330 mL in 1 VIAL, MULTI-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 36987-1314-4?

    The NDC Packaged Code 36987-1314-4 is assigned to a package of 50 ml in 1 vial, multi-dose of Cranberry, labeled by Nelco Laboratories, Inc.. The product's dosage form is and is administered via form.

    Is NDC 36987-1314 included in the NDC Directory?

    No, Cranberry with product code 36987-1314 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nelco Laboratories, Inc. on August 29, 1972 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 36987-1314-4?

    The 11-digit format is 36987131404. 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
    5-4-136987-1314-45-4-236987-1314-04