Details for New Drug Application (NDA): 090896
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The generic ingredient in CHLOROTHIAZIDE SODIUM is chlorothiazide sodium. There is one drug master file entry for this compound. Five suppliers are listed for this compound. Additional details are available on the chlorothiazide sodium profile page.
Summary for 090896
| Tradename: | CHLOROTHIAZIDE SODIUM |
| Applicant: | Fresenius Kabi Usa |
| Ingredient: | chlorothiazide sodium |
| Patents: | 0 |
Pharmacology for NDA: 090896
| Physiological Effect | Increased Diuresis |
Suppliers and Packaging for NDA: 090896
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CHLOROTHIAZIDE SODIUM | chlorothiazide sodium | INJECTABLE;INJECTION | 090896 | ANDA | Fresenius Kabi USA, LLC | 63323-658 | 63323-658-27 | 1 VIAL in 1 BOX (63323-658-27) / 18 mL in 1 VIAL |
| CHLOROTHIAZIDE SODIUM | chlorothiazide sodium | INJECTABLE;INJECTION | 090896 | ANDA | Fresenius Kabi USA, LLC | 63323-658 | 63323-658-20 | 1 VIAL in 1 BOX (63323-658-20) / 18 mL in 1 VIAL |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG BASE/VIAL | ||||
| Approval Date: | Oct 16, 2009 | TE: | AP | RLD: | No | ||||
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