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Protonix
Protonix - 21695-108-15 - (pantoprazoel sodium)
Drug Information of Protonix
| Product NDC: | 21695-108 |
| Proprietary Name: | Protonix |
| Non Proprietary Name: | pantoprazoel sodium |
| Active Ingredient(s): | 40 mg/1 & nbsp; pantoprazoel sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Protonix
| Product NDC: | 21695-108 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020987 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010828 |
Package Information of Protonix
| Package NDC: | 21695-108-15 |
| Package Description: | 15 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-108-15) |
NDC Information of Protonix
| NDC Code | 21695-108-15 |
| Proprietary Name | Protonix |
| Package Description | 15 TABLET, DELAYED RELEASE in 1 BOTTLE (21695-108-15) |
| Product NDC | 21695-108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pantoprazoel sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20010828 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PANTOPRAZOLE SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
