NDC Package 67510-0521-1 Night Time Gelcap

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:
67510-0521-1
Package Description:
1 BLISTER PACK in 1 BOX / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Night Time Gelcap
Usage Information:
Take only as directed-see Overdose warningdo not exceed 4 doses per 24 hoursadults and children 12 yrs and over2 GelCaps with water every 6 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use
11-Digit NDC Billing Format:
67510052101
NDC to RxNorm Crosswalk:
  • RxCUI: 1112865 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 5 MG Oral Capsule
  • RxCUI: 1112865 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 5 MG Oral Capsule
  • RxCUI: 1112865 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 5 MG Oral Capsule
  • Labeler Name:
    Kareway Product, Inc.
    Sample Package:
    No
    Start Marketing Date:
    06-01-2011
    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
    67510-0521-02 BLISTER PACK in 1 BOX / 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    67510-0521-21 BLISTER PACK in 1 BOX / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    67510-0521-42 BLISTER PACK in 1 BOX / 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67510-0521-1?

    The NDC Packaged Code 67510-0521-1 is assigned to a package of 1 blister pack in 1 box / 10 capsule, liquid filled in 1 blister pack of Night Time Gelcap, labeled by Kareway Product, Inc.. The product's dosage form is and is administered via form.

    Is NDC 67510-0521 included in the NDC Directory?

    No, Night Time Gelcap with product code 67510-0521 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Kareway Product, Inc. on June 01, 2011 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 67510-0521-1?

    The 11-digit format is 67510052101. 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
    5-4-167510-0521-15-4-267510-0521-01