Myferon 150 Forte (MARTIN EKWEALOR PHARMACEUTICALS, INC.)


Welcome to the PulseAid listing for the Myferon 150 Forte drug offered from MARTIN EKWEALOR PHARMACEUTICALS, INC.. This Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] 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: MARTIN EKWEALOR PHARMACEUTICALS, INC.
NON-PROPRIETARY NAME: IRON SUCROSE, FOLIC ACID, CYANOCOBALAMIN
SUBSTANCE NAME: IRON SUCROSE; FOLIC ACID; CYANOCOBALAMIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1996-12-01
END MARKETING DATE: 0000-00-00


Myferon 150 Forte HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMyferon 150 Forte from MARTIN EKWEALOR PHARMACEUTICALS, INC.
LABELER NAME: MARTIN EKWEALOR PHARMACEUTICALS, INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 150; 1; 25(mg/1; mg/1; ug/1)
START MARKETING DATE: 1996-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58607-112_24af9e28-be37-44a7-89c9-629f29b621e9
PRODUCT NDC: 58607-112
APPLICATION NUMBER:

Other IRON SUCROSE; FOLIC ACID; CYANOCOBALAMIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
MARTIN EKWEALOR PHARMACEUTICALS, INC.Myferon 150 Forte