| Product NDC: | 59148-020 |
| Proprietary Name: | SAMSCA |
| Non Proprietary Name: | tolvaptan |
| Active Ingredient(s): | 15 mg/1 & nbsp; tolvaptan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59148-020 |
| Labeler Name: | Otsuka America Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022275 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090519 |
| Package NDC: | 59148-020-50 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59148-020-50) > 10 TABLET in 1 BLISTER PACK |
| NDC Code | 59148-020-50 |
| Proprietary Name | SAMSCA |
| Package Description | 1 BLISTER PACK in 1 CARTON (59148-020-50) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 59148-020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tolvaptan |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090519 |
| Marketing Category Name | NDA |
| Labeler Name | Otsuka America Pharmaceutical Inc. |
| Substance Name | TOLVAPTAN |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |