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Chlorothiazide
Chlorothiazide - 0143-1210-10 - (Chlorothiazide)
Drug Information of Chlorothiazide
| Product NDC: | 0143-1210 |
| Proprietary Name: | Chlorothiazide |
| Non Proprietary Name: | Chlorothiazide |
| Active Ingredient(s): | 500 mg/1 & nbsp; Chlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorothiazide
| Product NDC: | 0143-1210 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087736 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050830 |
Package Information of Chlorothiazide
| Package NDC: | 0143-1210-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0143-1210-10) |
NDC Information of Chlorothiazide
| NDC Code | 0143-1210-10 |
| Proprietary Name | Chlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0143-1210-10) |
| Product NDC | 0143-1210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050830 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | CHLOROTHIAZIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
