Chlorothiazide Sodium (American Regent, Inc.)
Welcome to the PulseAid listing for the Chlorothiazide Sodium drug offered from American Regent, Inc.. This Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] 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: | American Regent, Inc. |
| NON-PROPRIETARY NAME: | Chlorothiazide Sodium |
| SUBSTANCE NAME: | CHLOROTHIAZIDE SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-04-01 |
| END MARKETING DATE: | 0000-00-00 |
Chlorothiazide Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Chlorothiazide Sodium from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/18mL) |
| START MARKETING DATE: | 2015-04-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-1820_614c7c90-6d95-436f-ac98-0281f03f01ff |
| PRODUCT NDC: | 0517-1820 |
| APPLICATION NUMBER: | ANDA202561 |
Other CHLOROTHIAZIDE SODIUM Pharmaceutical Manufacturers / Labelers:
