49348-924 NDC - SUNMARK ARTHRITIS 8 HOUR ()

Drug Information

Product NDC: 49348-924

Proprietary Name: Sunmark Arthritis 8 Hour

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sunmark
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/30/2002

Package Information

No. Package Code Package Description Billing Unit
149348-924-0950 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-924-09)EA
249348-924-10100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49348-924-10)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC49348-924The 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 NAMESunmark Arthritis 8 HourThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/30/2002This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESunmarkName 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