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Dexatran

Active substance: MAGNESIUM SULFATE HEPTAHYDRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM PANTOTHENATE, SODIUM ASCORBATE, THIAMINE MONONITRATE, ZINC SULFATE, MANGANESE SULFATE, FERROUS FUMARATE, CUPRIC SULFATE

CAPSULE · MAGNESIUM SULFATE HEPTAHYDRATE 6.9 mg/1, RIBOFLAVIN 6 mg/1, NIACINAMIDE 30 mg/1, PYRIDOXINE HYDROCHLORIDE 5 mg/1, FOLIC ACID 1 mg/1, CYANOCOBALAMIN 15 ug/1, CALCIUM PANTOTHENATE 10 mg/1, SODIUM ASCORBATE 200 mg/1, THIAMINE MONONITRATE 10 mg/1, ZINC SULFATE 18.2 mg/1, MANGANESE SULFATE 1.3 mg/1, FERROUS FUMARATE 18 mg/1, CUPRIC SULFATE .8 mg/1

United StatesActive

Marketing holder: PureTek Corporation

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
59088-643
Registration status
Active
Dispensing
Prescription only
Route
CUTANEOUS, ORAL
Sources
  • product · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 59088-643 · Verified 2026-10-09 · open in source