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  5. NDC Package Code: 65662-005-01 Alka-seltzer Original

NDC Package 65662-005-01 Alka-seltzer Original

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:
65662-005-01
Package Description:
6 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
Product Code:
65662-005
Proprietary Name:
Alka-seltzer Original
Usage Information:
Directionsfully dissove 2 tablets in 4 ounces of water before takingadults and children 12 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 8 tablets in 24 hoursadults 60 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 4 tablets in 24 hourschildren under 12 yearsconsult a doctor
11-Digit NDC Billing Format:
65662000501
NDC to RxNorm Crosswalk:
  • RxCUI: 1536675 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536675 - ASA 325 MG / Citric Acid 1000 MG / NaHCO3 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - Alka-Seltzer 325 MG / 1000 MG / 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet [Alka-Seltzer]
  • RxCUI: 1536680 - Alka-Seltzer (aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG) Effervescent Oral Tablet
    • Labeler Name:
    Bayer Bitterfeld Gmbh
    Sample Package:
    No
    Start Marketing Date:
    12-01-2008
    Listing Expiration Date:
    12-31-2020
    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 65662-005-01?

    The NDC Packaged Code 65662-005-01 is assigned to a package of 6 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Alka-seltzer Original, labeled by Bayer Bitterfeld Gmbh. The product's dosage form is and is administered via form.

    Is NDC 65662-005 included in the NDC Directory?

    No, Alka-seltzer Original with product code 65662-005 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Bayer Bitterfeld Gmbh on December 01, 2008 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 65662-005-01?

    The 11-digit format is 65662000501. 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
    5-3-265662-005-015-4-265662-0005-01