Home
>
National Drug Code (NDC)
>
Sankaijo
Sankaijo - 49873-404-01 - (docusate sodium, sennosides)
Drug Information of Sankaijo
| Product NDC: | 49873-404 |
| Proprietary Name: | Sankaijo |
| Non Proprietary Name: | docusate sodium, sennosides |
| Active Ingredient(s): | 8.33; 1.36 mg/1; mg/1 & nbsp; docusate sodium, sennosides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sankaijo
| Product NDC: | 49873-404 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20021220 |
Package Information of Sankaijo
| Package NDC: | 49873-404-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49873-404-01) > 150 TABLET in 1 BOTTLE |
NDC Information of Sankaijo
| NDC Code | 49873-404-01 |
| Proprietary Name | Sankaijo |
| Package Description | 1 BOTTLE in 1 CARTON (49873-404-01) > 150 TABLET in 1 BOTTLE |
| Product NDC | 49873-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | docusate sodium, sennosides |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20021220 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 8.33; 1.36 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
