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Vaseretic
Vaseretic - 0187-0146-01 - (enalapril maleate and hydrochlorothiazide)
Drug Information of Vaseretic
| Product NDC: | 0187-0146 |
| Proprietary Name: | Vaseretic |
| Non Proprietary Name: | enalapril maleate and hydrochlorothiazide |
| Active Ingredient(s): | 10; 25 mg/1; mg/1 & nbsp; enalapril maleate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vaseretic
| Product NDC: | 0187-0146 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019221 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19861031 |
Package Information of Vaseretic
| Package NDC: | 0187-0146-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0187-0146-01) |
NDC Information of Vaseretic
| NDC Code | 0187-0146-01 |
| Proprietary Name | Vaseretic |
| Package Description | 100 TABLET in 1 BOTTLE (0187-0146-01) |
| Product NDC | 0187-0146 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | enalapril maleate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19861031 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 10; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
