Home NDC 59088-167 Vitrexate
Product NDC 59088-167
11-digit product format 590880167
Labeler code 59088
Product ID 59088-167_f204b4b3-176f-8839-e053-2a95a90a7115
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Folic Acid
Dosage form TABLET
Route ORAL
Labeler PureTek Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-11-30
Substance .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELENIUM; THIAMINE MONONITRATE; VITAMIN A ACETATE; ZINC OXIDE
Active strength 30; 120; 200; 20; 35; 8; 1000; 200; 2.3; 45; 20; 20; 3.4; 55; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; ug/1; ug/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1
Pharmacologic classes Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Vitrexate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength .ALPHA.-TOCOPHEROL ACETATE, DL- 30 mg/1 MAGNESIUM OXIDE 120 mg/1 CHROMIUM NICOTINATE 200 mg/1 PYRIDOXINE HYDROCHLORIDE 20 ug/1 MOLYBDENUM 35 ug/1 SELENIUM 8 ug/1 CHOLECALCIFEROL 1000 ug/1 RIBOFLAVIN 200 mg/1 NIACINAMIDE 2.3 mg/1 ASCORBIC ACID 45 ug/1 FOLIC ACID 20 mg/1 CYANOCOBALAMIN 20 mg/1 CALCIUM CARBONATE 3.4 mg/1 VITAMIN A ACETATE 55 ug/1 THIAMINE MONONITRATE 3 mg/1 ZINC OXIDE 1500 ug/1 MANGANESE SULFATE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 17 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59088-167-54 Vitrexate 30 in 1 BOTTLE, PLASTIC TABLET 30 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-167 VITRANOL (FOLIC ACID) TABLET VITREXATE (FOLIC ACID) TABLET [PURETEK CORPORATION] 10 Current NDC, Legacy NDC, 1 package rows 20230112_b34fee43-bea9-45b7-e053-2a95a90aad4d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59088-167-54 59088016754 30 TABLET in 1 BOTTLE, PLASTIC (59088-167-54) 30 tablet 2020-11-30 0000-00-00 No No Current