Product NDC: | 68084-266 |
Proprietary Name: | Ramipril |
Non Proprietary Name: | ramipril |
Active Ingredient(s): | 2.5 mg/1 & nbsp; ramipril |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68084-266 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076549 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080122 |
Package NDC: | 68084-266-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (68084-266-01) > 10 CAPSULE in 1 BLISTER PACK (68084-266-11) |
NDC Code | 68084-266-01 |
Proprietary Name | Ramipril |
Package Description | 10 BLISTER PACK in 1 CARTON (68084-266-01) > 10 CAPSULE in 1 BLISTER PACK (68084-266-11) |
Product NDC | 68084-266 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ramipril |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20080122 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | RAMIPRIL |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |