Product NDC: | 0054-0111 |
Proprietary Name: | Perindopril Erbumine |
Non Proprietary Name: | Perindopril Erbumine |
Active Ingredient(s): | 4 mg/1 & nbsp; Perindopril Erbumine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-0111 |
Labeler Name: | Roxane Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090072 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091110 |
Package NDC: | 0054-0111-25 |
Package Description: | 100 TABLET in 1 BOTTLE (0054-0111-25) |
NDC Code | 0054-0111-25 |
Proprietary Name | Perindopril Erbumine |
Package Description | 100 TABLET in 1 BOTTLE (0054-0111-25) |
Product NDC | 0054-0111 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Perindopril Erbumine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091110 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc. |
Substance Name | PERINDOPRIL ERBUMINE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |