0722-7076 NDC - NABUMETONE 500 MG ()

Drug Information

Product NDC: 0722-7076

Proprietary Name: Nabumetone 500 mg

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Nexgen Pharma, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/4/2019

Package Information

No. Package Code Package Description Billing Unit
10722-7076-01100 TABLET, FILM COATED in 1 BOTTLE (0722-7076-01)
20722-7076-05500 TABLET, FILM COATED in 1 BOTTLE (0722-7076-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0722-7076The 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 NAMENabumetone 500 mgThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/4/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENexgen Pharma, Inc.Name 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