Prometa

Product NDC

59088-172

11-digit product format

590880172

Labeler code

59088

Product ID

59088-172_23faa6c9-f8fb-5180-e063-6394a90aeeb9

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

2021-01-11

Substance

.ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CHROMIUM NICOTINATE; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; MAGNESIUM OXIDE; MANGANESE SULFATE; MOLYBDENUM; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELENIUM; THIAMINE MONONITRATE; VITAMIN A ACETATE; ZINC OXIDE

Active strength

30; 120; 200; 20; 55; 45; 10; 27; 1000; 200; 2.6; 50; 20; 150; 50; 3.4; 70; 3; 1500; 25 mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; ug/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], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], 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