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PANTOPRAZOLE SODIUM
PANTOPRAZOLE SODIUM - 50436-8102-2 - (PANTOPRAZOLE SODIUM)
Drug Information of PANTOPRAZOLE SODIUM
| Product NDC: | 50436-8102 |
| 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: | 50436-8102 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091231 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110119 |
Package Information of PANTOPRAZOLE SODIUM
| Package NDC: | 50436-8102-2 |
| Package Description: | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-8102-2) |
NDC Information of PANTOPRAZOLE SODIUM
| NDC Code | 50436-8102-2 |
| Proprietary Name | PANTOPRAZOLE SODIUM |
| Package Description | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-8102-2) |
| Product NDC | 50436-8102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PANTOPRAZOLE SODIUM |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110119 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | PANTOPRAZOLE SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
