Tandem Plus (US Pharmaceutical Corporation)
Welcome to the PulseAid listing for the Tandem Plus drug offered from US Pharmaceutical Corporation. This Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],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: | US Pharmaceutical Corporation |
NON-PROPRIETARY NAME: | Ferrous Fumarate and Polysacchride Iron Vitamin Mineral Complex Supplement |
SUBSTANCE NAME: | FERROUS FUMARATE; FERROUS ASPARTO GLYCINATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; RIBOFLAVIN; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; NIACINAMIDE; CALCIUM PANTOTHENATE; ZINC SULFATE; MAGNESIUM SU |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],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: | 2006-06-17 |
END MARKETING DATE: | 0000-00-00 |
Tandem Plus HUMAN PRESCRIPTION DRUG Details:
Item Description | Tandem Plus from US Pharmaceutical Corporation |
LABELER NAME: | US Pharmaceutical Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 162; 115.2; 200; 10; 6; 5; 15; 30; 10; 18.2; 1.3; .8; 1(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: | 2006-06-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52747-902_6f3280b9-49e3-4ff2-9c07-80bd1fded4e4 |
PRODUCT NDC: | 52747-902 |
APPLICATION NUMBER: | |
Other FERROUS FUMARATE; FERROUS ASPARTO GLYCINATE; SODIUM ASCORBATE; THIAMINE MONONITRATE; RIBOFLAVIN; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; NIACINAMIDE; CALCIUM PANTOTHENATE; ZINC SULFATE; MAGNESIUM SU Pharmaceutical Manufacturers / Labelers: