PureFe OB Plus (PureTek Corporation)


Welcome to the PulseAid listing for the PureFe OB Plus drug offered from PureTek Corporation. This Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: PureTek Corporation
NON-PROPRIETARY NAME: Ferrous Fumarate and Polysaccharide Iron Complex
SUBSTANCE NAME: FERROUS FUMARATE; IRON DEXTRAN; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; MAGNESIUM SULFATE, UNSPECIF
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2011-06-01
END MARKETING DATE: 0000-00-00


PureFe OB Plus HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPureFe OB Plus from PureTek Corporation
LABELER NAME: PureTek Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 53; 53; 6; 30; 5; 1; 15; 10; 200; 10; 6.9; 18.2; .8; 1.3(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)
START MARKETING DATE: 2011-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59088-113_513d5b5f-1f99-42b6-8256-7c9de4b8d1a9
PRODUCT NDC: 59088-113
APPLICATION NUMBER:

Other FERROUS FUMARATE; IRON DEXTRAN; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; MAGNESIUM SULFATE, UNSPECIF Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
PureTek CorporationPureFe OB Plus