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  5. NDC Package Code: 43598-824-18 Acid Reducer Original Strength

NDC Package 43598-824-18 Acid Reducer Original Strength

Famotidine Tablet 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:
43598-824-18
Package Description:
1 BOTTLE in 1 CARTON / 180 TABLET in 1 BOTTLE
Product Code:
43598-824
Proprietary Name:
Acid Reducer Original Strength
Non-Proprietary Name:
Famotidine
Substance Name:
Famotidine
Usage Information:
Ranitidine is known as an H2 blocker. It works by reducing the amount of acid in your stomach. It is used to prevent and treat heartburn and other symptoms caused by too much acid in the stomach (acid indigestion). This drug has been withdrawn from the US market due to problems with safety. A possible cancer-causing impurity has been found in some ranitidine products.
11-Digit NDC Billing Format:
43598082418
NDC to RxNorm Crosswalk:
  • RxCUI: 199047 - famotidine 10 MG Oral Tablet
  • RxCUI: 310273 - famotidine 20 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Dr.reddys Laboratories 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):
  • FAMOTIDINE 10 mg/1
    • Pharmacologic Class(es):
  • Histamine H2 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-2 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA077367
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-01-2020
    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.

    Frequently Asked Questions

    What is NDC 43598-824-18?

    The NDC Packaged Code 43598-824-18 is assigned to a package of 1 bottle in 1 carton / 180 tablet in 1 bottle of Acid Reducer Original Strength, a human over the counter drug labeled by Dr.reddys Laboratories Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 43598-824 included in the NDC Directory?

    Yes, Acid Reducer Original Strength with product code 43598-824 is active and included in the NDC Directory. The product was first marketed by Dr.reddys Laboratories Inc. on September 01, 2020 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 43598-824-18?

    The 11-digit format is 43598082418. 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
    5-3-243598-824-185-4-243598-0824-18