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Chlorothiazide
Chlorothiazide - 63323-658-20 - (CHLOROTHIAZIDE SODIUM)
Drug Information of Chlorothiazide
| Product NDC: | 63323-658 |
| Proprietary Name: | Chlorothiazide |
| 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
| Product NDC: | 63323-658 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090896 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091021 |
Package Information of Chlorothiazide
| Package NDC: | 63323-658-20 |
| Package Description: | 1 VIAL in 1 BOX (63323-658-20) > 18 mL in 1 VIAL |
NDC Information of Chlorothiazide
| NDC Code | 63323-658-20 |
| Proprietary Name | Chlorothiazide |
| Package Description | 1 VIAL in 1 BOX (63323-658-20) > 18 mL in 1 VIAL |
| Product NDC | 63323-658 |
| 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 | 20091021 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CHLOROTHIAZIDE SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/18mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
