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Trandolapril
Trandolapril - 65862-165-99 - (Trandolapril)
Drug Information of Trandolapril
| Product NDC: | 65862-165 |
| Proprietary Name: | Trandolapril |
| Non Proprietary Name: | Trandolapril |
| Active Ingredient(s): | 2 mg/1 & nbsp; Trandolapril |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trandolapril
| Product NDC: | 65862-165 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078438 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070612 |
Package Information of Trandolapril
| Package NDC: | 65862-165-99 |
| Package Description: | 1000 TABLET in 1 BOTTLE (65862-165-99) |
NDC Information of Trandolapril
| NDC Code | 65862-165-99 |
| Proprietary Name | Trandolapril |
| Package Description | 1000 TABLET in 1 BOTTLE (65862-165-99) |
| Product NDC | 65862-165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trandolapril |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070612 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | TRANDOLAPRIL |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
