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  5. NDC Package Code: 46204-0007-0 Prochlorperazine

NDC Package 46204-0007-0 Prochlorperazine

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:
46204-0007-0
Package Description:
10 kg in 1 BOTTLE
Product Code:
46204-0007
Non-Proprietary Name:
Prochlorperazine
Substance Name:
Prochlorperazine
Usage Information:
This medication is used to treat severe nausea and vomiting from certain causes (for example, after surgery or cancer treatment). Prochlorperazine belongs to a class of drugs known as phenothiazines. This medication is not recommended for use in children younger than 2 years or in children going through surgery.
11-Digit NDC Billing Format:
46204000700
Product Type:
Bulk Ingredient
Labeler Name:
Trifarma S.p.a
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):
PROCHLORPERAZINE 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:
05-04-2012
Listing Expiration Date:
12-31-2026
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 46204-0007-0?

The NDC Packaged Code 46204-0007-0 is assigned to an UNFINISHED drug package of 10 kg in 1 bottle of Prochlorperazine, a bulk ingredient labeled by Trifarma S.p.a. The product's dosage form is powder and is administered via form.

Is NDC 46204-0007 included in the NDC Directory?

Yes, Prochlorperazine is an UNFINISHED PRODUCT with code 46204-0007 that is active and included in the NDC Directory. The product was first marketed by Trifarma S.p.a on May 04, 2012 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 11-digit format for NDC 46204-0007-0?

The 11-digit format is 46204000700. 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
5-4-146204-0007-05-4-246204-0007-00