United States · FDA National Drug Code directory

Venexa

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
59088-176_f204b6b0-92af-3c22-e053-2995a90ad0aa
Product NDC
59088-176
Form
TABLET
Composition / generic term
Folic Acid
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
20210129
Source listing expiry
20261231

Source-listed ingredients

  • .ALPHA.-TOCOPHEROL ACETATE, DL- — 30 mg/1
  • MAGNESIUM OXIDE — 200 mg/1
  • CHROMIUM NICOTINATE — 35 ug/1
  • PYRIDOXINE HYDROCHLORIDE — 20 mg/1
  • MOLYBDENUM — 45 ug/1
  • SELENIUM — 55 ug/1
  • CHOLECALCIFEROL — 20 ug/1
  • RIBOFLAVIN — 3.4 mg/1
  • NIACINAMIDE — 20 mg/1
  • ASCORBIC ACID — 120 mg/1
  • FOLIC ACID — 1000 ug/1
  • CYANOCOBALAMIN — 8 ug/1
  • CALCIUM CARBONATE — 200 mg/1
  • VITAMIN A ACETATE — 1500 ug/1
  • THIAMINE MONONITRATE — 3 mg/1
  • ZINC OXIDE — 25 mg/1
  • MANGANESE SULFATE — 2.3 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (59088-176-54) · 59088-176-54

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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