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44946-1015 NDC - LUDENT ()

Drug Information

Product NDC: 44946-1015

Proprietary Name: Ludent

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sancilio & Company Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/10/2009

Package Information

No. Package Code Package Description Billing Unit
144946-1015-260 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1015-2)
244946-1015-3120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1015-3)
344946-1015-630 TABLET, CHEWABLE in 1 BLISTER PACK (44946-1015-6)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44946-1015The 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 NAMELudentThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/10/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESancilio & Company IncName 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