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Enalapril Maleate and Hydrochlorothiazide
Enalapril Maleate and Hydrochlorothiazide - 60505-0209-1 - (Enalapril maleate and hydrochlorothiazide)
Drug Information of Enalapril Maleate and Hydrochlorothiazide
| Product NDC: | 60505-0209 |
| Proprietary Name: | Enalapril Maleate and Hydrochlorothiazide |
| 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 Enalapril Maleate and Hydrochlorothiazide
| Product NDC: | 60505-0209 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076486 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070619 |
Package Information of Enalapril Maleate and Hydrochlorothiazide
| Package NDC: | 60505-0209-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (60505-0209-1) |
NDC Information of Enalapril Maleate and Hydrochlorothiazide
| NDC Code | 60505-0209-1 |
| Proprietary Name | Enalapril Maleate and Hydrochlorothiazide |
| Package Description | 100 TABLET in 1 BOTTLE (60505-0209-1) |
| Product NDC | 60505-0209 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Enalapril maleate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070619 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| 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] |
