Dexatran

Product NDC

59088-643

11-digit product format

590880643

Labeler code

59088

Product ID

59088-643_22078fec-3885-36f9-e063-6294a90aba17

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Multivitamin

Dosage form

CAPSULE

Route

CUTANEOUS; ORAL

Labeler

PureTek Corporation

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2023-02-15

Substance

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

Active strength

10; .8; 15; 18; 1; 6.9; 1.3; 30; 5; 6; 200; 10; 18.2 mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; 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]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes