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ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE - 54868-5503-0 - (ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE)
Drug Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
| Product NDC: | 54868-5503 |
| Proprietary Name: | ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE |
| Active Ingredient(s): | 5; 12.5 g/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: | 54868-5503 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076486 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060110 |
Package Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
| Package NDC: | 54868-5503-0 |
| Package Description: | 30 TABLET in 1 BOTTLE (54868-5503-0) |
NDC Information of ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE
| NDC Code | 54868-5503-0 |
| Proprietary Name | ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE |
| Package Description | 30 TABLET in 1 BOTTLE (54868-5503-0) |
| Product NDC | 54868-5503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060110 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 5; 12.5 |
| Strength Unit | g/1; mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
