FERROUS SULFATE (MARTIN EKWEALOR PHARMACEUTICALS, INC.)


Welcome to the PulseAid listing for the FERROUS SULFATE drug offered from MARTIN EKWEALOR PHARMACEUTICALS, INC.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: MARTIN EKWEALOR PHARMACEUTICALS, INC.
NON-PROPRIETARY NAME: FERROUS SULFATE
SUBSTANCE NAME: FERROUS SULFATE; CALCIUM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2014-09-01
END MARKETING DATE: 0000-00-00


FERROUS SULFATE HUMAN OTC DRUG Details:

Item DescriptionFERROUS SULFATE from MARTIN EKWEALOR PHARMACEUTICALS, INC.
LABELER NAME: MARTIN EKWEALOR PHARMACEUTICALS, INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 65; 20(mg/1; mg/1)
START MARKETING DATE: 2014-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58607-113_07283557-cfb0-4689-8e9e-a0dd5c061fda
PRODUCT NDC: 58607-113
APPLICATION NUMBER:

Other FERROUS SULFATE; CALCIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
MARTIN EKWEALOR PHARMACEUTICALS, INC.FERROUS SULFATE