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  5. NDC Package Code: 76413-319-01 Mi-acid Regular Strength

NDC Package 76413-319-01 Mi-acid Regular Strength

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:
76413-319-01
Package Description:
355 mL in 1 BOTTLE
Product Code:
76413-319
Proprietary Name:
Mi-acid Regular Strength
Usage Information:
• shake well before use• adults and children 12 years and older: take 2 to 4 teaspoonfuls between meals, at bedtime, or as directed by a doctor• do not take more than 24 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks• children under 12 years: ask a doctor
11-Digit NDC Billing Format:
76413031901
NDC to RxNorm Crosswalk:
  • RxCUI: 210036 - Mi-Acid 200 MG / 200 MG / 20 MG in 5 mL Oral Suspension
  • RxCUI: 210036 - aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML / simethicone 4 MG/ML Oral Suspension [Mi-Acid]
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 20 MG) per 5 ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 40 MG / magnesium hydroxide 40 MG / simethicone 4 MG) per ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG) per 10 ML Oral Suspension
    • Labeler Name:
    Central Texas Community Health Centers
    Sample Package:
    No
    Start Marketing Date:
    02-01-2011
    Listing Expiration Date:
    12-31-2019
    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 76413-319-01?

    The NDC Packaged Code 76413-319-01 is assigned to a package of 355 ml in 1 bottle of Mi-acid Regular Strength, labeled by Central Texas Community Health Centers. The product's dosage form is and is administered via form.

    Is NDC 76413-319 included in the NDC Directory?

    No, Mi-acid Regular Strength with product code 76413-319 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Central Texas Community Health Centers on February 01, 2011 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 76413-319-01?

    The 11-digit format is 76413031901. 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
    5-3-276413-319-015-4-276413-0319-01