63739-432 NDC - SENNOSIDES AND DOCUSATE SODIUM ()

Drug Information

Product NDC: 63739-432

Proprietary Name: Sennosides and Docusate Sodium

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	McKesson Packaging Services a business unit of McKesson Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	10/11/2007

No.	Package Code	Package Description	Billing Unit
1	63739-432-02	30 BLISTER PACK in 1 BOX (63739-432-02) / 10 TABLET in 1 BLISTER PACK	EA

Field Name	Field Value	Definition
PRODUCT NDC	63739-432	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Sennosides and Docusate Sodium	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	10/11/2007	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	McKesson Packaging Services a business unit of McKesson Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023