1. Home
  2. Labeler Index
  3. Velocity Pharma
  4. 76168-057
  5. NDC Package Code: 76168-057-12 Daytime Nighttime Cold/flu

NDC Package 76168-057-12 Daytime Nighttime Cold/flu

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:
76168-057-12
Package Description:
1 KIT in 1 CARTON * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
76168-057
Proprietary Name:
Daytime Nighttime Cold/flu
Usage Information:
This product is used as Daytime Cold and Flu:pain relieverCough SuppressantNasal decongestantNighttime cold and flu purpose:pain relieverCough SuppressantAntihistamine. Daytime cold and flu: pain reliever, cough suppressant and Nasal decongestantNightTime Cold and Flu: pain reliever, cough suppressant and Antihistamine
11-Digit NDC Billing Format:
76168005712
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:
    Velocity Pharma
    Sample Package:
    No
    Start Marketing Date:
    07-15-2014
    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.

    Frequently Asked Questions

    What is NDC 76168-057-12?

    The NDC Packaged Code 76168-057-12 is assigned to a package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack * 4 capsule, liquid filled in 1 blister pack of Daytime Nighttime Cold/flu, labeled by Velocity Pharma. The product's dosage form is and is administered via form.

    Is NDC 76168-057 included in the NDC Directory?

    No, Daytime Nighttime Cold/flu with product code 76168-057 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Velocity Pharma on July 15, 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 76168-057-12?

    The 11-digit format is 76168005712. 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
    5-3-276168-057-125-4-276168-0057-12