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Docusate Sodium - 63739-478-01 - (Docusate Sodium)

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Drug Information of Docusate Sodium

Product NDC: 63739-478
Proprietary Name: Docusate Sodium
Non Proprietary Name: Docusate Sodium
Active Ingredient(s): 100    mg/1 & nbsp;   Docusate Sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Docusate Sodium

Product NDC: 63739-478
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20101108

Package Information of Docusate Sodium

Package NDC: 63739-478-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-478-01) > 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Docusate Sodium

NDC Code 63739-478-01
Proprietary Name Docusate Sodium
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-478-01) > 30 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 63739-478
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Docusate Sodium
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20101108
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name DOCUSATE SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Docusate Sodium


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