0615-7666 NDC - NABUMETONE ()

Drug Information

Product NDC: 0615-7666

Proprietary Name: Nabumetone

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/22/2010

Package Information

No. Package Code Package Description Billing Unit
10615-7666-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-7666-39)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0615-7666The 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 NAMENabumetoneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/22/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENCS HealthCare of KY, Inc dba Vangard LabsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/26/2021