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Pantoprazole Sodium
Pantoprazole Sodium - 62175-180-43 - (Pantoprazole Sodium)
Drug Information of Pantoprazole Sodium
| Product NDC: | 62175-180 |
| Proprietary Name: | Pantoprazole Sodium |
| Non Proprietary Name: | Pantoprazole Sodium |
| Active Ingredient(s): | 20 mg/1 & nbsp; Pantoprazole Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pantoprazole Sodium
| Product NDC: | 62175-180 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078281 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110120 |
Package Information of Pantoprazole Sodium
| Package NDC: | 62175-180-43 |
| Package Description: | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-180-43) |
NDC Information of Pantoprazole Sodium
| NDC Code | 62175-180-43 |
| Proprietary Name | Pantoprazole Sodium |
| Package Description | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-180-43) |
| Product NDC | 62175-180 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pantoprazole Sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110120 |
| Marketing Category Name | ANDA |
| Labeler Name | Kremers Urban Pharmaceuticals Inc. |
| Substance Name | PANTOPRAZOLE SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
