DIURIL is a Oral Suspension in the Human Prescription Drug category. It is labeled and distributed by Salix Pharmaceuticals, Inc. The primary component is Chlorothiazide.
Product ID | 65649-311_5431439b-abd5-4bc3-9873-8510f1ab9938 |
NDC | 65649-311 |
Product Type | Human Prescription Drug |
Proprietary Name | DIURIL |
Generic Name | Chlorothiazide |
Dosage Form | Suspension |
Route of Administration | ORAL |
Marketing Start Date | 1962-02-15 |
Marketing Category | NDA / NDA |
Application Number | NDA011870 |
Labeler Name | Salix Pharmaceuticals, Inc |
Substance Name | CHLOROTHIAZIDE |
Active Ingredient Strength | 250 mg/5mL |
Pharm Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1962-02-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA011870 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1962-02-15 |
Ingredient | Strength |
---|---|
CHLOROTHIAZIDE | 250 mg/5mL |
SPL SET ID: | bd936e35-1af8-42da-bcc0-f22489d68574 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
65649-311 | DIURIL | CHLOROTHIAZIDE |
0143-1209 | Chlorothiazide | Chlorothiazide |
0143-1210 | Chlorothiazide | Chlorothiazide |
0378-0150 | Chlorothiazide | chlorothiazide |
0378-0162 | Chlorothiazide | chlorothiazide |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIURIL 72051925 0676884 Live/Registered |
MERCK & CO., INC. 1958-05-19 |
DIURIL 72029293 0660963 Dead/Expired |
MERCK & CO., INC. 1957-05-02 |