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Dexatran

NDC 59088-643, Multivitamin, capsule, from PureTek Corporation.

Product NDC
59088-643
Status
Listed
Labeler
PureTek Corporation
Dosage form
CAPSULE
Route
CUTANEOUS, ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-643 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MAGNESIUM SULFATE HEPTAHYDRATE6.9 mg/1
  • RIBOFLAVIN6 mg/1
  • NIACINAMIDE30 mg/1
  • PYRIDOXINE HYDROCHLORIDE5 mg/1
  • FOLIC ACID1 mg/1
  • CYANOCOBALAMIN15 ug/1
  • CALCIUM PANTOTHENATE10 mg/1
  • SODIUM ASCORBATE200 mg/1
  • THIAMINE MONONITRATE10 mg/1
  • ZINC SULFATE18.2 mg/1
  • MANGANESE SULFATE1.3 mg/1
  • FERROUS FUMARATE18 mg/1
  • CUPRIC SULFATE.8 mg/1

Pharmacologic classes

Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Calculi Dissolution Agent [EPC]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [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 B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]

Package NDCNDC-11Package
59088-643-545908806435430 CAPSULE in 1 BOTTLE, PLASTIC (59088-643-54)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e052d2c2-7a3f-37be-e053-2a95a90af21c

Use it

Look up 59088-643 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-643 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-643. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.