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PANTOPRAZOLE SODIUM
PANTOPRAZOLE SODIUM - 17478-069-34 - (PANTOPRAZOLE SODIUM)
Drug Information of PANTOPRAZOLE SODIUM
| Product NDC: | 17478-069 |
| Proprietary Name: | PANTOPRAZOLE SODIUM |
| Non Proprietary Name: | PANTOPRAZOLE SODIUM |
| Active Ingredient(s): | 40 mg/1 & nbsp; PANTOPRAZOLE SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PANTOPRAZOLE SODIUM
| Product NDC: | 17478-069 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079197 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121108 |
Package Information of PANTOPRAZOLE SODIUM
| Package NDC: | 17478-069-34 |
| Package Description: | 10 VIAL in 1 CARTON (17478-069-34) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of PANTOPRAZOLE SODIUM
| NDC Code | 17478-069-34 |
| Proprietary Name | PANTOPRAZOLE SODIUM |
| Package Description | 10 VIAL in 1 CARTON (17478-069-34) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 17478-069 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PANTOPRAZOLE SODIUM |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20121108 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | PANTOPRAZOLE SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
