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CHLOROTHIAZIDE SODIUM
CHLOROTHIAZIDE SODIUM - 47335-330-40 - (CHLOROTHIAZIDE SODIUM)
Drug Information of CHLOROTHIAZIDE SODIUM
| Product NDC: | 47335-330 |
| Proprietary Name: | CHLOROTHIAZIDE SODIUM |
| Non Proprietary Name: | CHLOROTHIAZIDE SODIUM |
| Active Ingredient(s): | 500 mg/18mL & nbsp; CHLOROTHIAZIDE SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHLOROTHIAZIDE SODIUM
| Product NDC: | 47335-330 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091546 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110805 |
Package Information of CHLOROTHIAZIDE SODIUM
| Package NDC: | 47335-330-40 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) > 18 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of CHLOROTHIAZIDE SODIUM
| NDC Code | 47335-330-40 |
| Proprietary Name | CHLOROTHIAZIDE SODIUM |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) > 18 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 47335-330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLOROTHIAZIDE SODIUM |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110805 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | CHLOROTHIAZIDE SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/18mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
