Amiloride Hydrochloride (Carilion Materials Management)


Welcome to the PulseAid listing for the Amiloride Hydrochloride drug offered from Carilion Materials Management. This Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] 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: Carilion Materials Management
NON-PROPRIETARY NAME: Amiloride Hydrochloride
SUBSTANCE NAME: AMILORIDE HYDROCHLORIDE ANHYDROUS
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1986-01-22
END MARKETING DATE: 0000-00-00


Amiloride Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAmiloride Hydrochloride from Carilion Materials Management
LABELER NAME: Carilion Materials Management
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/1)
START MARKETING DATE: 1986-01-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68151-0162_3755be8b-624b-4bc4-958b-505220694dc1
PRODUCT NDC: 68151-0162
APPLICATION NUMBER: ANDA070346

Other AMILORIDE HYDROCHLORIDE ANHYDROUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Carilion Materials ManagementAmiloride Hydrochloride
Golden State Medical Supply, Inc.Amiloride Hydrochloride
Par Pharmaceutical Inc.Amiloride Hydrochloride