51096-0001 NDC - GLUTEN SENSITIVITY FORMULA ()

Drug Information

Product NDC: 51096-0001

Proprietary Name: Gluten Sensitivity Formula

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	51096-0001-1	180 mg in 1 BOTTLE (51096-0001-1)

Field Name	Field Value	Definition
PRODUCT NDC	51096-0001	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	Gluten Sensitivity Formula	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	3/1/2013	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	The Wise Alternative	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