Chlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceutical Corp. The primary component is Chlorothiazide.
| Product ID | 0143-1209_2af0405e-71c2-4074-bbd2-41ef19697dd0 |
| NDC | 0143-1209 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Chlorothiazide |
| Generic Name | Chlorothiazide |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2005-08-30 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA086028 |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | CHLOROTHIAZIDE |
| Active Ingredient Strength | 250 mg/1 |
| Pharm Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2005-08-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA086028 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-08-30 |
| Marketing End Date | 2014-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA086028 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2005-08-30 |
| Marketing End Date | 2014-10-31 |
| Ingredient | Strength |
|---|---|
| CHLOROTHIAZIDE | 250 mg/1 |
| SPL SET ID: | 32689670-ff81-40a1-8f2e-7a2de69cb603 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0143-1209 | Chlorothiazide | Chlorothiazide |
| 0143-1210 | Chlorothiazide | Chlorothiazide |
| 0378-0150 | Chlorothiazide | chlorothiazide |
| 0378-0162 | Chlorothiazide | chlorothiazide |
| 63323-658 | Chlorothiazide | CHLOROTHIAZIDE SODIUM |
| 65649-311 | DIURIL | CHLOROTHIAZIDE |