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  5. NDC Package Code: 45737-610-10 Biogesic

NDC Package 45737-610-10 Biogesic

Acetaminophen,Dexbrompheniramine Maleate Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
45737-610-10
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
45737-610
Proprietary Name:
Biogesic
Non-Proprietary Name:
Acetaminophen, Dexbrompheniramine Maleate
Substance Name:
Acetaminophen; Dexbrompheniramine Maleate
Usage Information:
UsesFor the temporary relief of minor aches and pains associated withheadachemuscular achesbackachesminor arthiritis paincommon coldtoothachesmentrual crampstemporarily reduces feveritchy and watery eyes due to hay fever
11-Digit NDC Billing Format:
45737061010
NDC to RxNorm Crosswalk:
  • RxCUI: 1798453 - acetaminophen 500 MG / dexbrompheniramine maleate 1 MG Oral Tablet
  • RxCUI: 1798453 - APAP 500 MG / Dexbrompheniramine maleate 1 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Advanced Generic Corporation
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETAMINOPHEN 500 mg/1
  • DEXBROMPHENIRAMINE MALEATE 1 mg/1
    • Sample Package:
    No
    FDA Application Number:
    part343
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    01-01-2017
    Listing Expiration Date:
    12-31-2024
    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 45737-610-10?

    The NDC Packaged Code 45737-610-10 is assigned to a package of 100 tablet in 1 bottle of Biogesic, a human over the counter drug labeled by Advanced Generic Corporation. The product's dosage form is tablet and is administered via oral form.

    Is NDC 45737-610 included in the NDC Directory?

    Yes, Biogesic with product code 45737-610 is active and included in the NDC Directory. The product was first marketed by Advanced Generic Corporation on January 01, 2017 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 45737-610-10?

    The 11-digit format is 45737061010. 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
    5-3-245737-610-105-4-245737-0610-10