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  5. NDC Package Code: 50742-191-01 Primaquine Phosphate

NDC Package 50742-191-01 Primaquine Phosphate

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50742-191-01
Package Description:
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
50742-191
Proprietary Name:
Primaquine Phosphate
Non-Proprietary Name:
Primaquine Phosphate
Substance Name:
Primaquine Phosphate
Usage Information:
Primaquine is used with other medications to prevent and treat malaria caused by mosquito bites in countries where malaria is common. Malaria parasites can enter the body through these mosquito bites, and then live in body tissues such as red blood cells or the liver. Primaquine is used after other medications (such as chloroquine) have killed the malaria parasites living inside red blood cells. Primaquine then kills the malaria parasites living in other body tissues. This prevents the return of the infection. Both drugs are needed for a complete cure. Primaquine phosphate belongs to a class of drugs known as antimalarials. The United States Centers for Disease Control provide updated guidelines and travel recommendations for the prevention and treatment of malaria in different parts of the world. Discuss the most recent information with your doctor before traveling to areas where malaria occurs.
11-Digit NDC Billing Format:
50742019101
NDC to RxNorm Crosswalk:
  • RxCUI: 904170 - primaquine phosphate 26.3 MG Oral Tablet
  • RxCUI: 904170 - primaquine phosphate 26.3 MG (primaquine 15 MG) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ingenus Pharmaceuticals, Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PRIMAQUINE PHOSPHATE 15 mg/1
    • Pharmacologic Class(es):
  • Antimalarial - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA206043
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-23-2018
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50742-191-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50742-191-01?

    The NDC Packaged Code 50742-191-01 is assigned to a package of 100 tablet, film coated in 1 bottle, plastic of Primaquine Phosphate, a human prescription drug labeled by Ingenus Pharmaceuticals, Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 50742-191 included in the NDC Directory?

    Yes, Primaquine Phosphate with product code 50742-191 is active and included in the NDC Directory. The product was first marketed by Ingenus Pharmaceuticals, Llc on January 23, 2018 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 50742-191-01?

    The 11-digit format is 50742019101. 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
    5-3-250742-191-015-4-250742-0191-01