| NDC Code | 51645-850-99 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (51645-850-99) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 51645-850 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Plus Pharma Senna Plus |
|---|
| Proprietary Name Suffix | Standardized Senna Concentrate 8.6 Mg And Docusate Sodium 50 Mg Each |
|---|
| Non-Proprietary Name | Docusate Sodium,sennosides |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060327 |
|---|
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
|---|
| Application Number | part334 |
|---|
| Manufacturer | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
|---|
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
|---|
| Strength | 50; 8.6 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|