PureVit DualFe Plus (PureTek Corporation)
Welcome to the PulseAid listing for the PureVit DualFe 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 Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],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, Polysaccharide Iron Complex |
SUBSTANCE NAME: | FERROUS FUMARATE; IRON DEXTRAN; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE; CUPRIC SULFAT |
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 Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],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 |
PureVit DualFe Plus HUMAN PRESCRIPTION DRUG Details:
Item Description | PureVit DualFe Plus from PureTek Corporation |
LABELER NAME: | PureTek Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 53; 53; 6; 30; 5; 1; 15; 10; 200; 10; 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) |
START MARKETING DATE: | 2011-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59088-112_4d17e61e-bc2a-42ca-a019-4f3801ba2108 |
PRODUCT NDC: | 59088-112 |
APPLICATION NUMBER: | |
Other FERROUS FUMARATE; IRON DEXTRAN; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC SULFATE; CUPRIC SULFAT Pharmaceutical Manufacturers / Labelers: