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AcipHex
AcipHex - 62856-243-30 - (rabeprazole sodium)
Drug Information of AcipHex
| Product NDC: | 62856-243 |
| Proprietary Name: | AcipHex |
| Non Proprietary Name: | rabeprazole sodium |
| Active Ingredient(s): | 20 mg/1 & nbsp; rabeprazole sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AcipHex
| Product NDC: | 62856-243 |
| Labeler Name: | Eisai Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020973 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990819 |
Package Information of AcipHex
| Package NDC: | 62856-243-30 |
| Package Description: | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62856-243-30) |
NDC Information of AcipHex
| NDC Code | 62856-243-30 |
| Proprietary Name | AcipHex |
| Package Description | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62856-243-30) |
| Product NDC | 62856-243 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rabeprazole sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19990819 |
| Marketing Category Name | NDA |
| Labeler Name | Eisai Inc. |
| Substance Name | RABEPRAZOLE SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
