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Sennosides and Docusate Sodium - 63739-432-10 - (Sennosides and Docusate Sodium)

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Drug Information of Sennosides and Docusate Sodium

Product NDC: 63739-432
Proprietary Name: Sennosides and Docusate Sodium
Non Proprietary Name: Sennosides and Docusate Sodium
Active Ingredient(s): 50; 8.6    mg/1; mg/1 & nbsp;   Sennosides and Docusate Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sennosides and Docusate Sodium

Product NDC: 63739-432
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20071011

Package Information of Sennosides and Docusate Sodium

Package NDC: 63739-432-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-432-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Sennosides and Docusate Sodium

NDC Code 63739-432-10
Proprietary Name Sennosides and Docusate Sodium
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-432-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-432
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sennosides and Docusate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071011
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name DOCUSATE SODIUM; SENNOSIDES
Strength Number 50; 8.6
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Sennosides and Docusate Sodium


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