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Enalapril Maleate and Hydrochlorothiazide
Enalapril Maleate and Hydrochlorothiazide - 51672-4046-3 - (Enalapril Maleate and Hydrochlorothiazide)
Drug Information of Enalapril Maleate and Hydrochlorothiazide
| Product NDC: | 51672-4046 |
| 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: | 51672-4046 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075788 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010918 |
Package Information of Enalapril Maleate and Hydrochlorothiazide
| Package NDC: | 51672-4046-3 |
| Package Description: | 1000 TABLET in 1 BOTTLE (51672-4046-3) |
NDC Information of Enalapril Maleate and Hydrochlorothiazide
| NDC Code | 51672-4046-3 |
| Proprietary Name | Enalapril Maleate and Hydrochlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE (51672-4046-3) |
| Product NDC | 51672-4046 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Enalapril Maleate and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010918 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 10; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
