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Aceon
Aceon - 76234-000-01 - (perindopril erbumine)
Drug Information of Aceon
| Product NDC: | 76234-000 |
| Proprietary Name: | Aceon |
| Non Proprietary Name: | perindopril erbumine |
| Active Ingredient(s): | 2 mg/1 & nbsp; perindopril erbumine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aceon
| Product NDC: | 76234-000 |
| Labeler Name: | XOMA (US) LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020184 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19931230 |
Package Information of Aceon
| Package NDC: | 76234-000-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (76234-000-01) |
NDC Information of Aceon
| NDC Code | 76234-000-01 |
| Proprietary Name | Aceon |
| Package Description | 100 TABLET in 1 BOTTLE (76234-000-01) |
| Product NDC | 76234-000 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | perindopril erbumine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19931230 |
| Marketing Category Name | NDA |
| Labeler Name | XOMA (US) LLC |
| Substance Name | PERINDOPRIL ERBUMINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
