Product NDC: | 0186-6040 |
Proprietary Name: | NEXIUM |
Non Proprietary Name: | Esomeprazole sodium |
Active Ingredient(s): | 40 mg/5mL & nbsp; Esomeprazole sodium |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0186-6040 |
Labeler Name: | AstraZeneca LP |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021689 |
Marketing Category: | NDA |
Start Marketing Date: | 20050503 |
Package NDC: | 0186-6040-01 |
Package Description: | 10 VIAL in 1 CARTON (0186-6040-01) > 5 mL in 1 VIAL |
NDC Code | 0186-6040-01 |
Proprietary Name | NEXIUM |
Package Description | 10 VIAL in 1 CARTON (0186-6040-01) > 5 mL in 1 VIAL |
Product NDC | 0186-6040 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Esomeprazole sodium |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20050503 |
Marketing Category Name | NDA |
Labeler Name | AstraZeneca LP |
Substance Name | ESOMEPRAZOLE SODIUM |
Strength Number | 40 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |