NDC Package 51552-1538-3 Imiquimod

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

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:
51552-1538-3
Package Description:
10 g in 1 CONTAINER
Product Code:
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:
51552153803
Product Type:
Bulk Ingredient
Labeler Name:
Fagron Inc
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):
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING - A category specifying that a bulk product is intended for use on humans and requires a prescription.
Start Marketing Date:
01-03-2018
End Marketing Date:
05-31-2027
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
51552-1538-21 g in 1 CONTAINER
51552-1538-425 g in 1 CONTAINER

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 51552-1538-3?

The NDC Packaged Code 51552-1538-3 is assigned to an UNFINISHED drug package of 10 g in 1 container of Imiquimod, a bulk ingredient labeled by Fagron Inc. The product's dosage form is powder and is administered via form.

Is NDC 51552-1538 included in the NDC Directory?

Yes, Imiquimod is an UNFINISHED PRODUCT with code 51552-1538 that is active and included in the NDC Directory. The product was first marketed by Fagron Inc on January 03, 2018.

What is the 11-digit format for NDC 51552-1538-3?

The 11-digit format is 51552153803. 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
5-4-151552-1538-35-4-251552-1538-03