Product NDC: | 55154-4232 |
Proprietary Name: | Protonix |
Non Proprietary Name: | pantoprazole sodium |
Active Ingredient(s): | 40 mg/1 & nbsp; pantoprazole sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, DELAYED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4232 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022020 |
Marketing Category: | NDA |
Start Marketing Date: | 20080229 |
Package NDC: | 55154-4232-0 |
Package Description: | 10 PACKET in 1 BAG (55154-4232-0) > 40 GRANULE, DELAYED RELEASE in 1 PACKET |
NDC Code | 55154-4232-0 |
Proprietary Name | Protonix |
Package Description | 10 PACKET in 1 BAG (55154-4232-0) > 40 GRANULE, DELAYED RELEASE in 1 PACKET |
Product NDC | 55154-4232 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | pantoprazole sodium |
Dosage Form Name | GRANULE, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20080229 |
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] |