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  5. NDC Package Code: 53943-614-05 Supreme Antacid

NDC Package 53943-614-05 Supreme Antacid

Calcium Carbonate,Magnesium Hydroxide Liquid 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:
53943-614-05
Package Description:
355 mL in 1 BOTTLE
Product Code:
53943-614
Proprietary Name:
Supreme Antacid
Non-Proprietary Name:
Calcium Carbonate, Magnesium Hydroxide
Substance Name:
Calcium Carbonate; Magnesium Hydroxide
Usage Information:
Shake well before useadults and children 12 years and older: take 2 to 4 teaspoonfuls two times a day, or as directed by a doctorchildren under 12 years: consult a doctor
11-Digit NDC Billing Format:
53943061405
NDC to RxNorm Crosswalk:
  • RxCUI: 237865 - calcium carbonate 400 MG / magnesium hydroxide 135 MG in 5 mL Oral Suspension
  • RxCUI: 237865 - calcium carbonate 80 MG/ML / magnesium hydroxide 27 MG/ML Oral Suspension
  • RxCUI: 237865 - calcium carbonate 400 MG / milk of magnesia 135 MG per 5 ML Oral Suspension
Product Type:
Human Otc Drug
Labeler Name:
Discount Drug Mart, Inc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M001
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-26-2025
Listing Expiration Date:
12-31-2026
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 53943-614-05?

The NDC Packaged Code 53943-614-05 is assigned to a package of 355 ml in 1 bottle of Supreme Antacid, a human over the counter drug labeled by Discount Drug Mart, Inc. The product's dosage form is liquid and is administered via oral form.

Is NDC 53943-614 included in the NDC Directory?

Yes, Supreme Antacid with product code 53943-614 is active and included in the NDC Directory. The product was first marketed by Discount Drug Mart, Inc on February 26, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 53943-614-05?

The 11-digit format is 53943061405. 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
5-3-253943-614-055-4-253943-0614-05