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  5. NDC Package Code: 59088-005-54 Multitol-m

NDC Package 59088-005-54 Multitol-m

Multivitamin,Folate 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:
59088-005-54
Package Description:
30 TABLET in 1 BOTTLE, PLASTIC
Product Code:
59088-005
Proprietary Name:
Multitol-m
Non-Proprietary Name:
Multivitamin, Folate
Substance Name:
.alpha.-tocopherol Acetate, Dl-; Ascorbic Acid; Calcium Carbonate; Cholecalciferol; Chromium Nicotinate; Levomefolate Calcium; Magnesium Oxide; Manganese Sulfate; Methylcobalamin; Molybdenum; Niacinamide; Pyridoxine Hydrochloride; Riboflavin; Selenium; Thiamine Mononitrate; Vitamin A Acetate; Zinc Oxide
Usage Information:
Multitol-M™ is indicated to provide vitamins and minerals supplement to men and women. Folate is effective in the treatment of megaloblastic anemias due to a deficiency of folate (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.
11-Digit NDC Billing Format:
59088000554
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
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.
Active Ingredient(s):
Pharmacologic Class(es):
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:
04-17-2024
Listing Expiration Date:
12-31-2025
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 59088-005-54?

The NDC Packaged Code 59088-005-54 is assigned to a package of 30 tablet in 1 bottle, plastic of Multitol-m, a human prescription drug labeled by Puretek Corporation. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

Is NDC 59088-005 included in the NDC Directory?

Yes, Multitol-m with product code 59088-005 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on April 17, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 59088-005-54?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 59088-005-54?

The 11-digit format is 59088000554. 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
5-3-259088-005-545-4-259088-0005-54