chlorothiazide sodium (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the chlorothiazide sodium drug offered from Sagent Pharmaceuticals. 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: | Sagent Pharmaceuticals |
| 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: | 2015-10-12 |
| END MARKETING DATE: | 0000-00-00 |
chlorothiazide sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | chlorothiazide sodium from Sagent Pharmaceuticals |
| LABELER NAME: | Sagent Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/18mL) |
| START MARKETING DATE: | 2015-10-12 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 25021-305_b3297614-fada-4119-86c9-8701a446f6c1 |
| PRODUCT NDC: | 25021-305 |
| APPLICATION NUMBER: | ANDA202462 |
Other CHLOROTHIAZIDE SODIUM Pharmaceutical Manufacturers / Labelers:
