NDC Package 59088-184-54 Dermacinrx Purefoltin

Folic Acid,Vitamin D3 Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

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:
59088-184-54
Package Description:
30 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Dermacinrx Purefoltin
Non-Proprietary Name:
Folic Acid, Vitamin D3
Substance Name:
Folic Acid; Vitamin D
Usage Information:
Purefoltin™ is indicated for dietary management of patients with unique nutritional needs requiring increased folate levels and Vitamin D supplementation. Purefoltin™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.
11-Digit NDC Billing Format:
59088018454
NDC to RxNorm Crosswalk:
  • RxCUI: 1720258 - vitamin D 3 125 MCG (5000 UNT) / folic acid 1 MG Oral Tablet
  • RxCUI: 1720258 - cholecalciferol 5000 UNT / folic acid 1 MG Oral Tablet
  • RxCUI: 1720258 - Cholecalciferol 5000 UNT / folate 1 MG Oral Tablet
  • RxCUI: 1720258 - vitamin D 3 125 MCG / folic acid 1000 MCG Oral Tablet
  • RxCUI: 1720258 - vitamin D 3 5000 UNT / folic acid 1 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Puretek Corporation
    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.
  • 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:
    05-03-2021
    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 59088-184-54?

    The NDC Packaged Code 59088-184-54 is assigned to a package of 30 tablet in 1 bottle, plastic of Dermacinrx Purefoltin, a human prescription drug labeled by Puretek Corporation. The product's dosage form is tablet and is administered via oral form.

    Is NDC 59088-184 included in the NDC Directory?

    Yes, Dermacinrx Purefoltin with product code 59088-184 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on May 03, 2021 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 59088-184-54?

    The 11-digit format is 59088018454. 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
    5-3-259088-184-545-4-259088-0184-54