NDC Package 41250-877-08 Nite Time Severe Cold And Flu Maximum Strength

Acetaminophen,Dextromethorphan Hbr,Doxylamine Succinate,Phenylephrine Hcl Tablet, Film - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
41250-877-08
Package Description:
2 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Nite Time Severe Cold And Flu Maximum Strength
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed do not take more than 8 caplets in 24 hours adults and children 12 years and over: take 2 caplets with water every 4 hours children under 12 years: ask a doctor
11-Digit NDC Billing Format:
41250087708
NDC to RxNorm Crosswalk:
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1546881 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer Distribution Inc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-01-2015
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    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 41250-877-08?

    The NDC Packaged Code 41250-877-08 is assigned to a package of 2 blister pack in 1 carton / 12 tablet, film coated in 1 blister pack of Nite Time Severe Cold And Flu Maximum Strength, a human over the counter drug labeled by Meijer Distribution Inc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 41250-877 included in the NDC Directory?

    Yes, Nite Time Severe Cold And Flu Maximum Strength with product code 41250-877 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution Inc on August 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41250-877-08?

    The 11-digit format is 41250087708. 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
    5-3-241250-877-085-4-241250-0877-08