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  5. NDC Package Code: 68016-490-40 Day-time Night-time

NDC Package 68016-490-40 Day-time Night-time

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
68016-490-40
Package Description:
1 KIT in 1 CARTON * 10 CAPSULE in 1 BLISTER PACK * 10 CAPSULE in 1 BLISTER PACK
Product Code:
68016-490
Proprietary Name:
Day-time Night-time
Usage Information:
Take only as recommended (see overdose warning)take Night-Time or Day-Time age Night-Time Day-Time adults and children 12 years of age and older swallow 2 softgels with water every 6 hours swallow 2 softgels with water every 4 hours children 4 to 12 years of age ask a doctor ask a doctor children under 4 years of age do not use do not useIf taking Night-Time and Day-Time softgels limit total to 4 doses per day
11-Digit NDC Billing Format:
68016049040
NDC to RxNorm Crosswalk:
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
    • Labeler Name:
    Chain Drug Consortium, Llc
    Sample Package:
    No
    Start Marketing Date:
    07-12-2010
    Listing Expiration Date:
    12-31-2018
    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.

    Frequently Asked Questions

    What is NDC 68016-490-40?

    The NDC Packaged Code 68016-490-40 is assigned to a package of 1 kit in 1 carton * 10 capsule in 1 blister pack * 10 capsule in 1 blister pack of Day-time Night-time, labeled by Chain Drug Consortium, Llc. The product's dosage form is and is administered via form.

    Is NDC 68016-490 included in the NDC Directory?

    No, Day-time Night-time with product code 68016-490 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Chain Drug Consortium, Llc on July 12, 2010 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68016-490-40?

    The 11-digit format is 68016049040. 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
    5-3-268016-490-405-4-268016-0490-40