PureFe OB Plus

Product NDC

59088-113

11-digit product format

590880113

Labeler code

59088

Product ID

59088-113_513d5b5f-1f99-42b6-8256-7c9de4b8d1a9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ferrous Fumarate and Polysaccharide Iron Complex

Dosage form

CAPSULE

Route

ORAL

Labeler

PureTek Corporation

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2011-06-01

Marketing end

0000-00-00

Substance

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

Active strength

53 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1

Pharmacologic classes

Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record