Product NDC: | 55154-4225 |
Proprietary Name: | Protonix |
Non Proprietary Name: | pantoprazole sodium |
Active Ingredient(s): | 40 mg/1 & nbsp; pantoprazole sodium |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4225 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020988 |
Marketing Category: | NDA |
Start Marketing Date: | 20010501 |
Package NDC: | 55154-4225-5 |
Package Description: | 5 VIAL in 1 BAG (55154-4225-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Code | 55154-4225-5 |
Proprietary Name | Protonix |
Package Description | 5 VIAL in 1 BAG (55154-4225-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
Product NDC | 55154-4225 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | pantoprazole sodium |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20010501 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | PANTOPRAZOLE SODIUM |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |