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  5. NDC Package Code: 55319-624-12 Supreme Antacid

NDC Package 55319-624-12 Supreme Antacid

Calcium Carbonate,Magnesium Hydroxide Suspension 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:
55319-624-12
Package Description:
355 mL in 1 BOTTLE
Product Code:
55319-624
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 between meals, at bedtime, or as directed by a doctordo not take more than 18 teaspoonfuls in a 24 hour period or use the maximum dosage for more than 2 weekschildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
55319062412
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:
Family Dollar Services Inc
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
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:
06-01-2017
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 55319-624-12?

The NDC Packaged Code 55319-624-12 is assigned to a package of 355 ml in 1 bottle of Supreme Antacid, a human over the counter drug labeled by Family Dollar Services Inc. The product's dosage form is suspension and is administered via oral form.

Is NDC 55319-624 included in the NDC Directory?

Yes, Supreme Antacid with product code 55319-624 is active and included in the NDC Directory. The product was first marketed by Family Dollar Services Inc on June 01, 2017 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 55319-624-12?

The 11-digit format is 55319062412. 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
5-3-255319-624-125-4-255319-0624-12