NDC Package 51655-440-52 Cyclobenzaprine Hydrochloride

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:
51655-440-52
Package Description:
30 TABLET in 1 BOTTLE, DISPENSING
Product Code:
Proprietary Name:
Cyclobenzaprine Hydrochloride
Usage Information:
Cyclobenzaprine HCl is indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions.Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living.Cyclobenzaprine HCl should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is generally of short duration and specific therapy for longer periods is seldom warranted.Cyclobenzaprine HCl has not been found effective in the treatment of spasticity associated with cerebral or spinal cord disease, or in children with cerebral palsy.
11-Digit NDC Billing Format:
51655044052
NDC to RxNorm Crosswalk:
  • RxCUI: 828348 - cyclobenzaprine HCl 10 MG Oral Tablet
  • RxCUI: 828348 - cyclobenzaprine hydrochloride 10 MG Oral Tablet
  • Labeler Name:
    Northwind Pharmaceuticals, Llc
    Sample Package:
    No
    Start Marketing Date:
    11-24-2014
    Listing Expiration Date:
    12-31-2019
    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
    51655-440-5415 TABLET in 1 BOTTLE, DISPENSING

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51655-440-52?

    The NDC Packaged Code 51655-440-52 is assigned to a package of 30 tablet in 1 bottle, dispensing of Cyclobenzaprine Hydrochloride, labeled by Northwind Pharmaceuticals, Llc. The product's dosage form is and is administered via form.

    Is NDC 51655-440 included in the NDC Directory?

    No, Cyclobenzaprine Hydrochloride with product code 51655-440 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Northwind Pharmaceuticals, Llc on November 24, 2014 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51655-440-52?

    The 11-digit format is 51655044052. 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
    5-3-251655-440-525-4-251655-0440-52