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  5. NDC Package Code: 84671-1030-0 Imiquimod

NDC Package 84671-1030-0 Imiquimod

Powder - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
84671-1030-0
Package Description:
1 kg in 1 CARTON
Product Code:
84671-1030
Non-Proprietary Name:
Imiquimod
Substance Name:
Imiquimod
Usage Information:
This medication is used to treat certain types of growths on the skin. These are precancerous growths (actinic keratoses), a certain type of skin cancer (superficial basal cell carcinoma), and warts on the outside of the genitals/anus. Treating these conditions can decrease complications from them. Imiquimod belongs to a group of drugs called immune response modifiers. It is believed to work by helping to activate your immune system to fight these abnormal skin growths. This product is not recommended for use on children under 12 years of age unless specifically directed by your doctor.
11-Digit NDC Billing Format:
84671103000
Product Type:
Bulk Ingredient
Labeler Name:
Tapi Hungary Industries Kft.
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
IMIQUIMOD 1 kg/kg
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
11-08-2010
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Unfinished Product:
Yes
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 84671-1030-0?

The NDC Packaged Code 84671-1030-0 is assigned to an UNFINISHED drug package of 1 kg in 1 carton of Imiquimod, a bulk ingredient labeled by Tapi Hungary Industries Kft.. The product's dosage form is powder and is administered via form.

Is NDC 84671-1030 included in the NDC Directory?

Yes, Imiquimod is an UNFINISHED PRODUCT with code 84671-1030 that is active and included in the NDC Directory. The product was first marketed by Tapi Hungary Industries Kft. on November 08, 2010 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 84671-1030-0?

The 11-digit format is 84671103000. 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 5-4-1 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
5-4-184671-1030-05-4-284671-1030-00