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Sodium Diuril
Sodium Diuril - 76478-711-40 - (chlorothiazide sodium)
Drug Information of Sodium Diuril
| Product NDC: | 76478-711 |
| Proprietary Name: | Sodium Diuril |
| Non Proprietary Name: | chlorothiazide sodium |
| Active Ingredient(s): | .5 mg/18mL & nbsp; chlorothiazide sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Diuril
| Product NDC: | 76478-711 |
| Labeler Name: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011145 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19581003 |
Package Information of Sodium Diuril
| Package NDC: | 76478-711-40 |
| Package Description: | 12 VIAL in 1 CARTON (76478-711-40) > 18 mL in 1 VIAL |
NDC Information of Sodium Diuril
| NDC Code | 76478-711-40 |
| Proprietary Name | Sodium Diuril |
| Package Description | 12 VIAL in 1 CARTON (76478-711-40) > 18 mL in 1 VIAL |
| Product NDC | 76478-711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorothiazide sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19581003 |
| Marketing Category Name | NDA |
| Labeler Name | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Substance Name | CHLOROTHIAZIDE SODIUM |
| Strength Number | .5 |
| Strength Unit | mg/18mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
