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Hydrochlorothiazide
Hydrochlorothiazide - 67253-821-55 - (Hydrochlorothiazide)
Drug Information of Hydrochlorothiazide
| Product NDC: | 67253-821 |
| Proprietary Name: | Hydrochlorothiazide |
| Non Proprietary Name: | Hydrochlorothiazide |
| Active Ingredient(s): | 50 mg/1 & nbsp; Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrochlorothiazide
| Product NDC: | 67253-821 |
| Labeler Name: | DAVA Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087068 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19801105 |
Package Information of Hydrochlorothiazide
| Package NDC: | 67253-821-55 |
| Package Description: | 5000 TABLET in 1 BOTTLE (67253-821-55) |
NDC Information of Hydrochlorothiazide
| NDC Code | 67253-821-55 |
| Proprietary Name | Hydrochlorothiazide |
| Package Description | 5000 TABLET in 1 BOTTLE (67253-821-55) |
| Product NDC | 67253-821 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19801105 |
| Marketing Category Name | ANDA |
| Labeler Name | DAVA Pharmaceuticals, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
