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Kapidex
Kapidex - 54868-5998-0 - (dexlansoprazole)
Drug Information of Kapidex
| Product NDC: | 54868-5998 |
| Proprietary Name: | Kapidex |
| Non Proprietary Name: | dexlansoprazole |
| Active Ingredient(s): | 30 mg/1 & nbsp; dexlansoprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kapidex
| Product NDC: | 54868-5998 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022287 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090305 |
Package Information of Kapidex
| Package NDC: | 54868-5998-0 |
| Package Description: | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (54868-5998-0) |
NDC Information of Kapidex
| NDC Code | 54868-5998-0 |
| Proprietary Name | Kapidex |
| Package Description | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (54868-5998-0) |
| Product NDC | 54868-5998 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dexlansoprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090305 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DEXLANSOPRAZOLE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
