FERROUS SULFATE (SPIRIT PHARMACEUTICALS,LLC)


Welcome to the PulseAid listing for the FERROUS SULFATE drug offered from SPIRIT PHARMACEUTICALS,LLC. 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: SPIRIT PHARMACEUTICALS,LLC
NON-PROPRIETARY NAME: FERROUS SULFATE, DRIED
SUBSTANCE NAME: FERROUS SULFATE, DRIED
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2010-12-15
END MARKETING DATE: 0000-00-00


FERROUS SULFATE HUMAN OTC DRUG Details:

Item DescriptionFERROUS SULFATE from SPIRIT PHARMACEUTICALS,LLC
LABELER NAME: SPIRIT PHARMACEUTICALS,LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 325(mg/1)
START MARKETING DATE: 2010-12-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68210-1520_0fe4df43-f430-4cf1-9033-43387e7db002
PRODUCT NDC: 68210-1520
APPLICATION NUMBER:

Other FERROUS SULFATE, DRIED Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
SPIRIT PHARMACEUTICALS,LLCFERROUS SULFATE