Aluminum Hydroxide (LLC Federal Solutions)


Welcome to the PulseAid listing for the Aluminum Hydroxide drug offered from LLC Federal Solutions. 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: LLC Federal Solutions
NON-PROPRIETARY NAME: Aluminum Hydroxide
SUBSTANCE NAME: ALUMINUM HYDROXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-08-12
END MARKETING DATE: 0000-00-00


Aluminum Hydroxide HUMAN OTC DRUG Details:

Item DescriptionAluminum Hydroxide from LLC Federal Solutions
LABELER NAME: LLC Federal Solutions
DEA SCHEDULE:
ACTIVE STRENGTH: 320(mg/5mL)
START MARKETING DATE: 2013-08-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24451-091_18de8a4b-df09-498a-ab6b-df914a59e48a
PRODUCT NDC: 24451-091
APPLICATION NUMBER: part331

Other ALUMINUM HYDROXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Atlantic Biologicals CorpsAluminum Hydroxide
DermaRite Industries, LLCDermaMed
GERITREX LLCDermadrox
LLC Federal SolutionsAluminum Hydroxide
McKesson Medical-SurgicalDERMA GRAN
Rugby Laboratories, Inc.Aluminum Hydroxide