55648-725 NDC - DIVALPROEX SODIUM ()

Drug Information

Product NDC: 55648-725

Proprietary Name: DIVALPROEX SODIUM

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	55648-725-01	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-01)
2	55648-725-02	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-02)
3	55648-725-03	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-725-03)
4	55648-725-04	10 BLISTER PACK in 1 CARTON (55648-725-04) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Field Name	Field Value	Definition
PRODUCT NDC	55648-725	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	DIVALPROEX SODIUM	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	ER	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE	8/4/2009	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	WOCKHARDT LIMITED	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