Aluminum Hydroxide (Rugby Laboratories, Inc.)


Welcome to the PulseAid listing for the Aluminum Hydroxide drug offered from Rugby Laboratories, 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: Rugby Laboratories, Inc.
NON-PROPRIETARY NAME: aluminum hydroxide
SUBSTANCE NAME: ALUMINUM HYDROXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2005-02-01
END MARKETING DATE: 0000-00-00


Aluminum Hydroxide HUMAN OTC DRUG Details:

Item DescriptionAluminum Hydroxide from Rugby Laboratories, Inc.
LABELER NAME: Rugby Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 320(mg/5mL)
START MARKETING DATE: 2005-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0536-0091_0c4d5b0e-bbd4-4089-bd86-28c7a7d1f5a3
PRODUCT NDC: 0536-0091
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