SODIUM HYDROXIDE (Gordon Laboratories)


Welcome to the PulseAid listing for the SODIUM HYDROXIDE drug offered from Gordon Laboratories. This Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Gordon Laboratories
NON-PROPRIETARY NAME: SODIUM HYDROXIDE
SUBSTANCE NAME: SODIUM HYDROXIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
ROUTE: TOPICAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2010-07-16
END MARKETING DATE: 0000-00-00


SODIUM HYDROXIDE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSODIUM HYDROXIDE from Gordon Laboratories
LABELER NAME: Gordon Laboratories
DEA SCHEDULE:
ACTIVE STRENGTH: 0.01(g/g)
START MARKETING DATE: 2010-07-16
END MARKETING DATE: 0000-00-00
PRODUCT ID: 10481-3006_b92631c2-5e63-4526-acdc-a2940145407b
PRODUCT NDC: 10481-3006
APPLICATION NUMBER:

Other SODIUM HYDROXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Gordon LaboratoriesSODIUM HYDROXIDE