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 DescriptionTandem Plus from US Pharmaceutical Corporation
LABELER NAME: US Pharmaceutical Corporation
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
US Pharmaceutical CorporationTandem Plus