Senokot-S 50 mg/1
standardized senna concentrate and docusate sodium · TABLET · Atlantis Consumer Healthcare, Inc.
Senokot-S is a tablet containing standardized senna concentrate and docusate sodium at 50 mg/1, taken oral. Manufactured by Atlantis Consumer Healthcare, Inc..
Key Facts
- Brand Name
- Senokot-S
- Generic Name
- standardized senna concentrate and docusate sodium
- NDC Code (Product)
67618-310- Manufacturer
- Atlantis Consumer Healthcare, Inc.
- Strength
- 50 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- M007
- Marketing Start
- 10/01/1974
Recall History
No Recall HistoryFrequently Asked Questions
What is Senokot-S used for?
Senokot-S contains standardized senna concentrate and docusate sodium. It is a tablet taken oral. Consult your doctor for specific uses.
Is Senokot-S a controlled substance?
Senokot-S is not classified as a controlled substance by the DEA.
What is the generic name for Senokot-S?
The generic name for Senokot-S is standardized senna concentrate and docusate sodium. There are no other listed brand versions of standardized senna concentrate and docusate sodium.
What is the NDC code for Senokot-S 50 mg/1?
The NDC (National Drug Code) for Senokot-S 50 mg/1 is 67618-310, listed by Atlantis Consumer Healthcare, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)