Home NDC 59088-177 Venexa FE
Product NDC 59088-177
11-digit product format 590880177
Labeler code 59088
Product ID 59088-177_f204c835-2fb4-27b1-e053-2995a90a43b9
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ferrous Fumarate, Folic Acid
Dosage form TABLET
Route ORAL
Labeler PureTek Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2021-01-29
Substance .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; 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; 27; 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; mg/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 Venexa FE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength 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
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 18 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 59088-177-54 Venexa FE 30 in 1 BOTTLE, PLASTIC TABLET 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-177 VENEXA FE (FERROUS FUMARATE, FOLIC ACID) TABLET [PURETEK CORPORATION] 5 Current NDC, Legacy NDC, 1 package rows 20230112_ba142128-21c4-4204-e053-2a95a90ae0d7.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Venexa FE FERROUS FUMARATE, FOLIC ACID PureTek Corporation ba142128-21c4-4204-e053-2a95a90ae0d7 2023-01-11 Warnings, Adverse reactions Exact identifier ndc (product): 59088-177
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59088-177-54 59088017754 30 TABLET in 1 BOTTLE, PLASTIC (59088-177-54) 30 tablet 2021-01-29 0000-00-00 No No Current