1. Home
  2. Labeler Index
  3. Trifluent Pharma, Llc
  4. 73352-051
  5. NDC Package Code: 73352-051-10 Pruradik

NDC Package 73352-051-10 Pruradik

Crotamiton Lotion Topical - 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:
73352-051-10
Package Description:
237 g in 1 BOTTLE, PLASTIC
Product Code:
73352-051
Proprietary Name:
Pruradik
Non-Proprietary Name:
Crotamiton
Substance Name:
Crotamiton
Usage Information:
This medication is used to treat scabies. Scabies is a skin infection caused by mites that burrow into the skin. Irritation from the mites leads to severe itching and small bumps/blisters filled with fluid/pus. Crotamiton works by killing the mites that cause scabies. It also helps relieve itching related to scabies and other skin conditions. Crotamiton belongs to two classes of drugs: scabicides and antipruritics.
11-Digit NDC Billing Format:
73352005110
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
237 GM
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Trifluent Pharma, Llc
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
CROTAMITON 100 mg/g
Sample Package:
No
FDA Application Number:
ANDA087204
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-02-2025
Listing Expiration Date:
12-31-2026
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 73352-051-10?

The NDC Packaged Code 73352-051-10 is assigned to a package of 237 g in 1 bottle, plastic of Pruradik, a human prescription drug labeled by Trifluent Pharma, Llc. The product's dosage form is lotion and is administered via topical form.This product is billed per "GM" gram and contains an estimated amount of 237 billable units per package.

Is NDC 73352-051 included in the NDC Directory?

Yes, Pruradik with product code 73352-051 is active and included in the NDC Directory. The product was first marketed by Trifluent Pharma, Llc on June 02, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 73352-051-10?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 237.

What is the 11-digit format for NDC 73352-051-10?

The 11-digit format is 73352005110. 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
5-3-273352-051-105-4-273352-0051-10