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SENNOSIDES AND DOCUSATE SODIUM
SENNOSIDES AND DOCUSATE SODIUM - 49483-097-01 - (SENNOSIDES AND DOCUSATE SODIUM)
Drug Information of SENNOSIDES AND DOCUSATE SODIUM
| Product NDC: | 49483-097 |
| Proprietary Name: | SENNOSIDES AND DOCUSATE SODIUM |
| Non Proprietary Name: | SENNOSIDES AND DOCUSATE SODIUM |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; SENNOSIDES AND DOCUSATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENNOSIDES AND DOCUSATE SODIUM
| Product NDC: | 49483-097 |
| Labeler Name: | TIME CAP LABORATORIES, INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of SENNOSIDES AND DOCUSATE SODIUM
| Package NDC: | 49483-097-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-097-01) |
NDC Information of SENNOSIDES AND DOCUSATE SODIUM
| NDC Code | 49483-097-01 |
| Proprietary Name | SENNOSIDES AND DOCUSATE SODIUM |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-097-01) |
| Product NDC | 49483-097 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SENNOSIDES AND DOCUSATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TIME CAP LABORATORIES, INC |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
