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  5. NDC Package Code: 59088-630-00 Naprotin

NDC Package 59088-630-00 Naprotin

Naproxen ,Capsaicin Kit - 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:
59088-630-00
Package Description:
1 KIT in 1 KIT * 100 TABLET in 1 BOTTLE (50228-436-01) * 237 mL in 1 BOTTLE, PUMP (59088-310-16)
Product Code:
59088-630
Proprietary Name:
Naprotin
Non-Proprietary Name:
Naproxen , Capsaicin
Usage Information:
Naproxen Tablets are indicated for: the relief of the signs and symptoms of: rheumatoid arthritisosteoarthritisankylosing spondylitispolyarticular juvenile idiopathic arthritistendonitisbursitis acute goutthe management of:painprimary dysmenorrhea
11-Digit NDC Billing Format:
59088063000
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 198014 - naproxen 500 MG Oral Tablet
  • RxCUI: 198555 - capsaicin 0.025 % Topical Cream
  • RxCUI: 198555 - capsaicin 0.25 MG/ML Topical Cream
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Puretek Corporation
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    09-27-2022
    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 59088-630-00?

    The NDC Packaged Code 59088-630-00 is assigned to a package of 1 kit in 1 kit * 100 tablet in 1 bottle (50228-436-01) * 237 ml in 1 bottle, pump (59088-310-16) of Naprotin, a human prescription drug labeled by Puretek Corporation. The product's dosage form is kit and is administered via form.

    Is NDC 59088-630 included in the NDC Directory?

    Yes, Naprotin with product code 59088-630 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on September 27, 2022 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 NDC billing unit for package 59088-630-00?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 59088-630-00?

    The 11-digit format is 59088063000. 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
    5-3-259088-630-005-4-259088-0630-00