Amiloride Hydrochloride (Par Pharmaceutical Inc.)
Welcome to the PulseAid listing for the Amiloride Hydrochloride drug offered from Par Pharmaceutical Inc.. 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: | Par Pharmaceutical Inc. |
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 Description | Amiloride Hydrochloride from Par Pharmaceutical Inc. |
LABELER NAME: | Par Pharmaceutical Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 1986-01-22 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49884-117_08c10863-8287-43be-9775-cf9f2a7a3b17 |
PRODUCT NDC: | 49884-117 |
APPLICATION NUMBER: | ANDA070346 |
Other AMILORIDE HYDROCHLORIDE ANHYDROUS Pharmaceutical Manufacturers / Labelers: