Docusate Plus Senna is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Safecor Health, Llc. The primary component is Docusate Sodium; Sennosides A And B.
Product ID | 48433-304_8d0c5a61-4d68-44d1-a600-0261c221daa9 |
NDC | 48433-304 |
Product Type | Human Otc Drug |
Proprietary Name | Docusate Plus Senna |
Generic Name | Docusate Sodium-sennosides |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2014-09-30 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part334 |
Labeler Name | Safecor Health, LLC |
Substance Name | DOCUSATE SODIUM; SENNOSIDES A AND B |
Active Ingredient Strength | 50 mg/1; min/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2014-11-10 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part334 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-09-30 |
Marketing End Date | 2019-11-11 |
Marketing Category | OTC monograph not final |
Application Number | part334 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-11-10 |
Marketing End Date | 2019-11-11 |
Marketing Category | OTC monograph not final |
Application Number | part334 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-09-30 |
Marketing End Date | 2019-11-11 |
Ingredient | Strength |
---|---|
DOCUSATE SODIUM | 50 mg/1 |
SPL SET ID: | 9e0d04b2-bef8-4adf-aee4-c0fd2d62c84f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
48433-304 | Docusate Plus Senna | DOCUSATE SODIUM-SENNOSIDES |
49483-081 | SENNA TIME S | DOCUSATE SODIUM-SENNOSIDES |