68134-601 NDC - FENOFIBRIC ACID ()

Drug Information

Product NDC: 68134-601

Proprietary Name: Fenofibric Acid

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Palmetto Pharmaceuticals, Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	10/7/2020

No.	Package Code	Package Description	Billing Unit
1	68134-601-30	30 TABLET in 1 BOTTLE, PLASTIC (68134-601-30)	EA

Field Name	Field Value	Definition
PRODUCT NDC	68134-601	The 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 NAME	Fenofibric Acid	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	10/7/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Palmetto Pharmaceuticals, Inc	Name 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