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  5. NDC Package Code: 63029-222-04 Tagamet

NDC Package 63029-222-04 Tagamet

Cimetidine Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
63029-222-04
Package Description:
4 BLISTER PACK in 1 BOX / 10 TABLET in 1 BLISTER PACK
Product Code:
63029-222
Proprietary Name:
Tagamet
Non-Proprietary Name:
Cimetidine
Substance Name:
Cimetidine
Usage Information:
Cimetidine is used to treat ulcers of the stomach and intestines and prevent them from coming back after they have healed. This medication is also used to treat certain stomach and throat (esophagus) problems caused by too much stomach acid (e.g., Zollinger-Ellison syndrome, erosive esophagitis) or a backward flow of stomach acid into the esophagus (acid reflux disease/GERD). Decreasing extra stomach acid can help relieve symptoms such as stomach pain, heartburn, difficulty swallowing, persistent cough, and trouble sleeping. It can also prevent serious acid damage to your digestive system (e.g., ulcers, cancer of the esophagus). Cimetidine belongs to a class of drugs commonly called H2 blockers. It works by reducing the amount of acid in your stomach. This medication is also available without a prescription. It is used to treat occasional heartburn caused by too much acid in the stomach (also called acid indigestion or sour stomach). It is also used to prevent heartburn and acid indigestion caused by certain foods and beverages. If you are taking this medication for self-treatment, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions.)
11-Digit NDC Billing Format:
63029022204
NDC to RxNorm Crosswalk:
  • RxCUI: 104062 - Tagamet HB 200 MG Oral Tablet
  • RxCUI: 104062 - cimetidine 200 MG Oral Tablet [Tagamet]
  • RxCUI: 104062 - Tagamet 200 MG Oral Tablet
  • RxCUI: 197505 - cimetidine 200 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Medtech Products 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):
  • CIMETIDINE 200 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:
    NDA020238
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-01-2012
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63029-222-011 BLISTER PACK in 1 BOX / 30 TABLET in 1 BLISTER PACK
    63029-222-021 BLISTER PACK in 1 BOX / 6 TABLET in 1 BLISTER PACK
    63029-222-031 BLISTER PACK in 1 BOX / 50 TABLET in 1 BLISTER PACK
    63029-222-054 BLISTER PACK in 1 BOX / 9 TABLET in 1 BLISTER PACK
    63029-222-067 BLISTER PACK in 1 BOX / 10 TABLET in 1 BLISTER PACK
    63029-222-091 BOTTLE in 1 CARTON / 90 TABLET in 1 BOTTLE
    63029-222-111 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
    63029-222-122 BLISTER PACK in 1 BOX / 6 TABLET in 1 BLISTER PACK
    63029-222-701 BOTTLE in 1 CARTON / 70 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63029-222-04?

    The NDC Packaged Code 63029-222-04 is assigned to a package of 4 blister pack in 1 box / 10 tablet in 1 blister pack of Tagamet, a human over the counter drug labeled by Medtech Products Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 63029-222 included in the NDC Directory?

    Yes, Tagamet with product code 63029-222 is active and included in the NDC Directory. The product was first marketed by Medtech Products Inc. on June 01, 2012 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 63029-222-04?

    The 11-digit format is 63029022204. 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
    5-3-263029-222-045-4-263029-0222-04