Home
>
National Drug Code (NDC)
>
DIURIL
DIURIL - 65649-311-12 - (CHLOROTHIAZIDE)
Drug Information of DIURIL
| Product NDC: | 65649-311 |
| Proprietary Name: | DIURIL |
| Non Proprietary Name: | CHLOROTHIAZIDE |
| Active Ingredient(s): | 250 mg/5mL & nbsp; CHLOROTHIAZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIURIL
| Product NDC: | 65649-311 |
| Labeler Name: | Salix Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011870 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19620215 |
Package Information of DIURIL
| Package NDC: | 65649-311-12 |
| Package Description: | 237 mL in 1 BOTTLE (65649-311-12) |
NDC Information of DIURIL
| NDC Code | 65649-311-12 |
| Proprietary Name | DIURIL |
| Package Description | 237 mL in 1 BOTTLE (65649-311-12) |
| Product NDC | 65649-311 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLOROTHIAZIDE |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19620215 |
| Marketing Category Name | NDA |
| Labeler Name | Salix Pharmaceuticals, Inc. |
| Substance Name | CHLOROTHIAZIDE |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
