Vitrexyl Plus Iron Tablet
NDC Package 59088-165-54
Package Information
Vitrexyl Plus Iron (ferrous fumarate, folic acid) tablets is vitrexyl + Iron is indicated for the treatment of iron deficiency anemia and folate deficiency as in extended convalescence, menorrhagia, pregnancy, puberty, excessive blood loss and advanced age.Also for treatment of condition in which iron deficiency and vitamin C deficiency occur together, alongwith a deficient intake or increased need for B-Complex vitamins in chronic and acute illness, as well ascases of metabolic stress, and in convalescence. This formulation utilizes a tablet delivery system. Marketed by Puretek Corporation, this product is identified by NDC 59088-165.
Identification & Billing
Clinical Specifications
- CHROMIUM NICOTINATE 30 mg/1
- FOLIC ACID 120 mg/1
- VITAMIN A ACETATE 200 mg/1
- RIBOFLAVIN 20 ug/1
- NIACINAMIDE 35 ug/1
- PYRIDOXINE HYDROCHLORIDE 8 ug/1
- CYANOCOBALAMIN 27 mg/1
- CALCIUM CARBONATE 1000 ug/1
- ASCORBIC ACID 200 mg/1
- THIAMINE MONONITRATE 2.3 mg/1
- ZINC OXIDE 45 ug/1
- MANGANESE SULFATE 20 mg/1
- FERROUS FUMARATE 20 mg/1
- MAGNESIUM OXIDE 3.4 mg/1
- MOLYBDENUM 55 ug/1
- .ALPHA.-TOCOPHEROL ACETATE, DL- 3 mg/1
- CHOLECALCIFEROL 1500 ug/1
- SELENIUM 25 mg/1
- 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)
Regulatory & Marketing
Hierarchy Structure
- 59088 - Puretek Corporation
- 59088-165 - Vitrexyl Plus Iron
- 59088-165-54 - 30 TABLET in 1 BOTTLE, PLASTIC
- 59088-165 - Vitrexyl Plus Iron
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 59088-165-54 identifies a specific commercial package of 30 tablet in 1 bottle, plastic of Vitrexyl Plus Iron, a human prescription drug labeled by Puretek Corporation. This tablet is formulated for oral use and contains chromium nicotinate; folic acid; vitamin a acetate; riboflavin; niacinamide; pyridoxine hydrochloride; cyanocobalamin; calcium carbonate; ascorbic acid; thiamine mononitrate; zinc oxide; manganese sulfate; ferrous fumarate; magnesium oxide; molybdenum; .alpha.-tocopherol acetate, dl-; cholecalciferol; selenium as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Puretek Corporation on August 24, 2020. The current certification is valid through December 31, 2026.
How is this Puretek Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59088016554. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.