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Docusate Sodium and Senna - 0536-0355-10 - (Docusate Sodium and Senna)

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Drug Information of Docusate Sodium and Senna

Product NDC: 0536-0355
Proprietary Name: Docusate Sodium and Senna
Non Proprietary Name: Docusate Sodium and Senna
Active Ingredient(s): 50; 8.6    mg/1; mg/1 & nbsp;   Docusate Sodium and Senna
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Docusate Sodium and Senna

Product NDC: 0536-0355
Labeler Name: Rugby Laboratories, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110922

Package Information of Docusate Sodium and Senna

Package NDC: 0536-0355-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0536-0355-10)

NDC Information of Docusate Sodium and Senna

NDC Code 0536-0355-10
Proprietary Name Docusate Sodium and Senna
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0536-0355-10)
Product NDC 0536-0355
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Docusate Sodium and Senna
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110922
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rugby Laboratories, Inc
Substance Name DOCUSATE SODIUM; SENNOSIDES
Strength Number 50; 8.6
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Docusate Sodium and Senna


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