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Protonix
Protonix - 0008-0923-55 - (PANTOPRAZOLE SODIUM)
Drug Information of Protonix
| Product NDC: | 0008-0923 |
| Proprietary Name: | Protonix |
| Non Proprietary Name: | PANTOPRAZOLE SODIUM |
| Active Ingredient(s): | 40 mg/10mL & nbsp; PANTOPRAZOLE SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Protonix
| Product NDC: | 0008-0923 |
| Labeler Name: | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020988 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010501 |
Package Information of Protonix
| Package NDC: | 0008-0923-55 |
| Package Description: | 10 CARTON in 1 PACKAGE (0008-0923-55) > 1 VIAL in 1 CARTON (0008-0923-51) > 10 mL in 1 VIAL |
NDC Information of Protonix
| NDC Code | 0008-0923-55 |
| Proprietary Name | Protonix |
| Package Description | 10 CARTON in 1 PACKAGE (0008-0923-55) > 1 VIAL in 1 CARTON (0008-0923-51) > 10 mL in 1 VIAL |
| Product NDC | 0008-0923 |
| 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 | Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc. |
| Substance Name | PANTOPRAZOLE SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
