NDC Package 17714-025-10 Antacid

Calcium Carbonate Tablet Oral - 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:
17714-025-10
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Antacid
Non-Proprietary Name:
Calcium Carbonate
Substance Name:
Calcium Carbonate
Usage Information:
This medication is used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
11-Digit NDC Billing Format:
17714002510
NDC to RxNorm Crosswalk:
  • RxCUI: 577040 - calcium carbonate 648 MG (Ca 260 MG) Oral Tablet
  • RxCUI: 577040 - calcium carbonate 648 MG Oral Tablet
  • RxCUI: 577040 - calcium carbonate 648 MG (as calcium 260 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Advance Pharmaceutical Inc.
    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):
    Sample Package:
    No
    FDA Application Number:
    part331
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    04-06-1990
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    17714-025-01100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17714-025-10?

    The NDC Packaged Code 17714-025-10 is assigned to a package of 1000 tablet in 1 bottle of Antacid, a human over the counter drug labeled by Advance Pharmaceutical Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 17714-025 included in the NDC Directory?

    Yes, Antacid with product code 17714-025 is active and included in the NDC Directory. The product was first marketed by Advance Pharmaceutical Inc. on April 06, 1990 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 17714-025-10?

    The 11-digit format is 17714002510. 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
    5-3-217714-025-105-4-217714-0025-10