Sodium Diuril is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Akorn. The primary component is Chlorothiazide Sodium.
| Product ID | 76478-711_2800c4be-9fc3-49f8-ad03-b75d9a4ca9a9 |
| NDC | 76478-711 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sodium Diuril |
| Generic Name | Chlorothiazide Sodium |
| Dosage Form | Injection |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 1958-10-03 |
| Marketing Category | NDA / NDA |
| Application Number | NDA011145 |
| Labeler Name | Akorn |
| Substance Name | CHLOROTHIAZIDE SODIUM |
| Active Ingredient Strength | 1 mg/18mL |
| Pharm Classes | Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 1958-10-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA011145 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1958-10-03 |
| Ingredient | Strength |
|---|---|
| CHLOROTHIAZIDE SODIUM | .5 mg/18mL |
| SPL SET ID: | 1d9fa4e6-6516-45cd-a316-292c6a529ecc |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 76478-711 | Sodium Diuril | chlorothiazide sodium |
| 63323-658 | Chlorothiazide | CHLOROTHIAZIDE SODIUM |
| 0517-1820 | Chlorothiazide Sodium | Chlorothiazide Sodium |
| 17478-419 | Chlorothiazide Sodium | Chlorothiazide Sodium |
| 25021-305 | chlorothiazide sodium | chlorothiazide sodium |
| 47335-330 | CHLOROTHIAZIDE SODIUM | CHLOROTHIAZIDE SODIUM |
| 67457-263 | chlorothiazide sodium | chlorothiazide sodium |