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Enalaprilat
Enalaprilat - 0703-8401-04 - (enalaprilat)
Drug Information of Enalaprilat
| Product NDC: | 0703-8401 |
| 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) |
Labeler Information of Enalaprilat
| Product NDC: | 0703-8401 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075578 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051006 |
Package Information of Enalaprilat
| Package NDC: | 0703-8401-04 |
| Package Description: | 25 VIAL in 1 TRAY (0703-8401-04) > 1 mL in 1 VIAL (0703-8401-01) |
NDC Information of Enalaprilat
| NDC Code | 0703-8401-04 |
| Proprietary Name | Enalaprilat |
| Package Description | 25 VIAL in 1 TRAY (0703-8401-04) > 1 mL in 1 VIAL (0703-8401-01) |
| Product NDC | 0703-8401 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | enalaprilat |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20051006 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc |
| 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] |
