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  5. NDC Package Code: 59088-166-54 Prenatrix

NDC Package 59088-166-54 Prenatrix

Ferrous Fumarate,Folic Acid 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:
59088-166-54
Package Description:
30 TABLET in 1 BOTTLE, PLASTIC
Product Code:
59088-166
Proprietary Name:
Prenatrix
Non-Proprietary Name:
Ferrous Fumarate, Folic Acid
Substance Name:
.alpha.-tocopherol Acetate, Dl-; Ascorbic Acid; Calcium Carbonate; Cholecalciferol; Choline Bitartrate; Chromium Nicotinate; Cyanocobalamin; Ferrous Fumarate; Folic Acid; Magnesium Oxide; Manganese Sulfate; Molybdenum; Niacinamide; Potassium Iodide; Pyridoxine Hydrochloride; Riboflavin; Selenium; Thiamine Mononitrate; Vitamin A Acetate; Zinc Oxide
Usage Information:
Prenatrix is indicated to provide vitamins and minerals to women throughout pregnancy and during the postnatal period for both lactating and non-lactating mothers, and throughout the childbearing years. Prenatrix may be beneficial in improving the nutritional status of women prior to conception.
11-Digit NDC Billing Format:
59088016654
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):
  • .ALPHA.-TOCOPHEROL ACETATE, DL- 30 mg/1
  • ASCORBIC ACID 120 mg/1
  • CALCIUM CARBONATE 200 mg/1
  • CHOLECALCIFEROL 20 ug/1
  • CHOLINE BITARTRATE 55 mg/1
  • CHROMIUM NICOTINATE 45 ug/1
  • CYANOCOBALAMIN 10 ug/1
  • FERROUS FUMARATE 27 mg/1
  • FOLIC ACID 1000 ug/1
  • MAGNESIUM OXIDE 200 mg/1
  • MANGANESE SULFATE 2.6 mg/1
  • MOLYBDENUM 50 ug/1
  • NIACINAMIDE 20 mg/1
  • POTASSIUM IODIDE 150 ug/1
  • PYRIDOXINE HYDROCHLORIDE 50 mg/1
  • RIBOFLAVIN 3.4 mg/1
  • SELENIUM 70 ug/1
  • THIAMINE MONONITRATE 3 mg/1
  • VITAMIN A ACETATE 1500 ug/1
  • ZINC OXIDE 25 mg/1
    • Pharmacologic Class(es):
  • Analogs/Derivatives - [Chemical/Ingredient]
  • Ascorbic Acid - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cations, Divalent - [CS]
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin A - [CS]
  • Vitamin A - [EPC] (Established Pharmacologic Class)
  • Vitamin B 12 - [CS]
  • Vitamin B 6 - [Chemical/Ingredient]
  • Vitamin B12 - [EPC] (Established Pharmacologic Class)
  • Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
  • Vitamin D - [CS]
  • Vitamin D - [EPC] (Established Pharmacologic Class)
    • 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:
    08-29-2020
    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 59088-166-54?

    The NDC Packaged Code 59088-166-54 is assigned to a package of 30 tablet in 1 bottle, plastic of Prenatrix, a human prescription drug labeled by Puretek Corporation. The product's dosage form is tablet and is administered via oral form.

    Is NDC 59088-166 included in the NDC Directory?

    Yes, Prenatrix with product code 59088-166 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on August 29, 2020 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 59088-166-54?

    The 11-digit format is 59088016654. 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
    5-3-259088-166-545-4-259088-0166-54