Product NDC: | 55154-0355 |
Proprietary Name: | Enalaprilat |
Non Proprietary Name: | Enalaprilat |
Active Ingredient(s): | 1.25 mg/mL & nbsp; Enalaprilat |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-0355 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075634 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000823 |
Package NDC: | 55154-0355-5 |
Package Description: | 5 VIAL in 1 BAG (55154-0355-5) > 1 mL in 1 VIAL |
NDC Code | 55154-0355-5 |
Proprietary Name | Enalaprilat |
Package Description | 5 VIAL in 1 BAG (55154-0355-5) > 1 mL in 1 VIAL |
Product NDC | 55154-0355 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Enalaprilat |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20000823 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | ENALAPRILAT |
Strength Number | 1.25 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |