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Enalapril maleate and hydrochlorothiazide
Enalapril maleate and hydrochlorothiazide - 55111-134-10 - (Enalapril maleate and hydrochlorothiazide)
Drug Information of Enalapril maleate and hydrochlorothiazide
| Product NDC: | 55111-134 |
| 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: | 55111-134 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075909 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011015 |
Package Information of Enalapril maleate and hydrochlorothiazide
| Package NDC: | 55111-134-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (55111-134-10) |
NDC Information of Enalapril maleate and hydrochlorothiazide
| NDC Code | 55111-134-10 |
| Proprietary Name | Enalapril maleate and hydrochlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE (55111-134-10) |
| Product NDC | 55111-134 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Enalapril maleate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20011015 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 10; 25 |
| Strength Unit | mg/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] |
