PureFe Plus (PureTek Corporation)
Welcome to the PulseAid listing for the PureFe 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 |
| SUBSTANCE NAME: | FERROUS FUMARATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; MAGNESIUM SULFATE, UNSPECIFIED; ZINC SULF |
| 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 Plus HUMAN PRESCRIPTION DRUG Details:
| Item Description | PureFe Plus from PureTek Corporation |
| LABELER NAME: | PureTek Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 106; 10; 6; 30; 5; 1; 15; 10; 200; 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) |
| START MARKETING DATE: | 2011-06-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59088-114_d726c3d0-9d1f-43ea-8971-30ecba0e87b7 |
| PRODUCT NDC: | 59088-114 |
| APPLICATION NUMBER: | |
Other FERROUS FUMARATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM PANTOTHENATE; SODIUM ASCORBATE; MAGNESIUM SULFATE, UNSPECIFIED; ZINC SULF Pharmaceutical Manufacturers / Labelers:
