NDC Package 49873-402-01 Inon Ace

Magnesium Aluminosilicates,Magnesium Hydroxide,Simethicone 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:
49873-402-01
Package Description:
1 BOTTLE in 1 CARTON / 75 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Inon Ace
Non-Proprietary Name:
Magnesium Aluminosilicates, Magnesium Hydroxide, Simethicone
Substance Name:
Dimethicone; Magnesium Hydroxide; Silodrate
Usage Information:
Uses relieves these symptoms ■heartburn ■acid indigestion ■sour stomach ■upset stomach and gas associated with these symptoms
11-Digit NDC Billing Format:
49873040201
NDC to RxNorm Crosswalk:
  • RxCUI: 1235450 - aluminum magnesium silicate 200 MG / magnesium hydroxide 60 MG / simethicone 20 MG Oral Tablet
  • RxCUI: 1235456 - INON ACE TABLETS 200 MG / 60 MG / 20 MG Oral Tablet
  • RxCUI: 1235456 - aluminum magnesium silicate 200 MG / magnesium hydroxide 60 MG / simethicone 20 MG Oral Tablet [Inon Ace Tablet]
  • RxCUI: 1235456 - Inon Ace Tablet (aluminum magnesium silicate 200 MG / magnesium hydroxide 60 MG / simethicone 20 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Sato Pharmaceutical Co., Ltd.
    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.
  • Sample Package:
    No
    FDA Application Number:
    M001
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-01-1995
    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.

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    Frequently Asked Questions

    What is NDC 49873-402-01?

    The NDC Packaged Code 49873-402-01 is assigned to a package of 1 bottle in 1 carton / 75 tablet in 1 bottle of Inon Ace, a human over the counter drug labeled by Sato Pharmaceutical Co., Ltd.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 49873-402 included in the NDC Directory?

    Yes, Inon Ace with product code 49873-402 is active and included in the NDC Directory. The product was first marketed by Sato Pharmaceutical Co., Ltd. on November 01, 1995 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 49873-402-01?

    The 11-digit format is 49873040201. 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
    5-3-249873-402-015-4-249873-0402-01