NDC Code | 55150-202-25 |
Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00) |
Product NDC | 55150-202 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Pantoprazole Sodium |
Non-Proprietary Name | Pantoprazole Sodium |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20160330 |
Marketing Category Name | ANDA |
Application Number | ANDA205675 |
Manufacturer | Eugia US LLC |
Substance Name | PANTOPRAZOLE SODIUM |
Strength | 40 |
Strength Unit | mg/1 |
Pharmacy Classes | Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |