| NDC Code | 51645-850-06 |
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| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-850-06) |
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| Product NDC | 51645-850 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Plus Pharma Senna Plus |
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| Proprietary Name Suffix | Standardized Senna Concentrate 8.6 Mg And Docusate Sodium 50 Mg Each |
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| Non-Proprietary Name | Docusate Sodium,sennosides |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20060327 |
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| End Marketing Date | 20220331 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part334 |
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| Manufacturer | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
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| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
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| Strength | 50; 8.6 |
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| Strength Unit | mg/1; mg/1 |
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