Domeboro (MOBERG PHARMA NORTH AMERICA LLC)


Welcome to the PulseAid listing for the Domeboro drug offered from MOBERG PHARMA NORTH AMERICA 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: MOBERG PHARMA NORTH AMERICA LLC
NON-PROPRIETARY NAME: Aluminum Sulfate Tetradecahydrate, Calcium Acetate Monohydrate
SUBSTANCE NAME: ALUMINUM SULFATE TETRADECAHYDRATE; CALCIUM ACETATE MONOHYDRATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2012-06-26
END MARKETING DATE: 0000-00-00


Domeboro HUMAN OTC DRUG Details:

Item DescriptionDomeboro from MOBERG PHARMA NORTH AMERICA LLC
LABELER NAME: MOBERG PHARMA NORTH AMERICA LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1347; 952(mg/1; mg/1)
START MARKETING DATE: 2012-06-26
END MARKETING DATE: 0000-00-00
PRODUCT ID: 16864-240_33d94df2-6c51-a2f7-9318-837d794f9127
PRODUCT NDC: 16864-240
APPLICATION NUMBER: part347

Other ALUMINUM SULFATE TETRADECAHYDRATE; CALCIUM ACETATE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
MOBERG PHARMA NORTH AMERICA LLCDomeboro