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ENALAPRIL MALEATE
ENALAPRIL MALEATE - 50436-4352-1 - (ENALAPRIL MALEATE)
Drug Information of ENALAPRIL MALEATE
| Product NDC: | 50436-4352 |
| Proprietary Name: | ENALAPRIL MALEATE |
| Non Proprietary Name: | ENALAPRIL MALEATE |
| Active Ingredient(s): | 20 mg/1 & nbsp; ENALAPRIL MALEATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ENALAPRIL MALEATE
| Product NDC: | 50436-4352 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075483 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091211 |
Package Information of ENALAPRIL MALEATE
| Package NDC: | 50436-4352-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (50436-4352-1) |
NDC Information of ENALAPRIL MALEATE
| NDC Code | 50436-4352-1 |
| Proprietary Name | ENALAPRIL MALEATE |
| Package Description | 30 TABLET in 1 BOTTLE (50436-4352-1) |
| Product NDC | 50436-4352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ENALAPRIL MALEATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091211 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | ENALAPRIL MALEATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
