| NDC Code | 47335-330-40 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 47335-330 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Chlorothiazide Sodium |
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| Non-Proprietary Name | Chlorothiazide Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20160825 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091546 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | CHLOROTHIAZIDE SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/18mL |
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| Pharmacy Classes | Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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