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 |