61919-160 NDC - NABUMETONE ()

Drug Information

Product NDC: 61919-160

Proprietary Name: NABUMETONE

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Direct Rx
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2015

Package Information

No. Package Code Package Description Billing Unit
161919-160-3030 BOTTLE in 1 BOTTLE (61919-160-30) > 60 TABLET, FILM COATED in 1 BOTTLE (61919-160-60)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC61919-160The 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 DATE1/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDirect RxName 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