Chlorothiazide (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Chlorothiazide drug offered from Fresenius Kabi USA, LLC. 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: | Fresenius Kabi USA, LLC |
| 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: | 2009-10-21 |
| END MARKETING DATE: | 0000-00-00 |
Chlorothiazide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Chlorothiazide from Fresenius Kabi USA, LLC |
| LABELER NAME: | Fresenius Kabi USA, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/18mL) |
| START MARKETING DATE: | 2009-10-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-658_2c482eda-8793-4bf5-80af-69cd10e7ff26 |
| PRODUCT NDC: | 63323-658 |
| APPLICATION NUMBER: | ANDA090896 |
Other CHLOROTHIAZIDE SODIUM Pharmaceutical Manufacturers / Labelers:
