| NDC Code | 51655-500-52 |
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| Package Description | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, DISPENSING (51655-500-52) |
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| Product NDC | 51655-500 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pantoprazole Sodium Delayed Release |
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| Non-Proprietary Name | Pantoprazole Sodium Delayed Release |
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| Dosage Form | TABLET, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140321 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090970 |
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| Manufacturer | Northwind Pharmaceuticals |
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| Substance Name | PANTOPRAZOLE SODIUM |
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| Strength | 40 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
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