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  5. NDC Package Code: 54348-989-06 Prochlorperazine

NDC Package 54348-989-06 Prochlorperazine

Tablet Oral - 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:
54348-989-06
Package Description:
1 BOTTLE in 1 BOX / 6 TABLET in 1 BOTTLE
Product Code:
54348-989
Proprietary Name:
Prochlorperazine
Non-Proprietary Name:
Prochlorperazine
Substance Name:
Prochlorperazine Maleate
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:
54348098906
NDC to RxNorm Crosswalk:
  • RxCUI: 312635 - prochlorperazine maleate 5 MG Oral Tablet
  • RxCUI: 312635 - prochlorperazine 5 MG Oral Tablet
  • RxCUI: 312635 - prochlorperazine 5 MG (as prochlorperazine maleate) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Pharmpak, 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):
  • PROCHLORPERAZINE MALEATE 5 mg/1
    • Pharmacologic Class(es):
  • Phenothiazine - [EPC] (Established Pharmacologic Class)
  • Phenothiazines - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA040268
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-11-2019
    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.

    Frequently Asked Questions

    What is NDC 54348-989-06?

    The NDC Packaged Code 54348-989-06 is assigned to a package of 1 bottle in 1 box / 6 tablet in 1 bottle of Prochlorperazine, a human prescription drug labeled by Pharmpak, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 54348-989 included in the NDC Directory?

    Yes, Prochlorperazine with product code 54348-989 is active and included in the NDC Directory. The product was first marketed by Pharmpak, Inc. on July 11, 2019 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 54348-989-06?

    The 11-digit format is 54348098906. 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
    5-3-254348-989-065-4-254348-0989-06