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Perindopril Erbumine
Perindopril Erbumine - 68180-235-01 - (Perindopril Erbumine)
Drug Information of Perindopril Erbumine
| Product NDC: | 68180-235 |
| Proprietary Name: | Perindopril Erbumine |
| 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 Perindopril Erbumine
| Product NDC: | 68180-235 |
| Labeler Name: | Lupin Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078263 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100315 |
Package Information of Perindopril Erbumine
| Package NDC: | 68180-235-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (68180-235-01) |
NDC Information of Perindopril Erbumine
| NDC Code | 68180-235-01 |
| Proprietary Name | Perindopril Erbumine |
| Package Description | 100 TABLET in 1 BOTTLE (68180-235-01) |
| Product NDC | 68180-235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Perindopril Erbumine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100315 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc |
| Substance Name | PERINDOPRIL ERBUMINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
