50436-0676 NDC - DICLOFENAC SODIUM ()

Drug Information

Product NDC: 50436-0676

Proprietary Name: Diclofenac Sodium

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Unit Dose Services
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/6/2002

Package Information

No. Package Code Package Description Billing Unit
150436-0676-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50436-0676-1)EA
250436-0676-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50436-0676-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50436-0676The 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 NAMEDiclofenac SodiumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/6/2002This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUnit Dose ServicesName 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