67046-230 NDC - GEMFIBROZIL ()

Drug Information

Product NDC: 67046-230

Proprietary Name: Gemfibrozil

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Contract Pharmacy Services-PA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/5/2010

Package Information

No. Package Code Package Description Billing Unit
167046-230-3030 TABLET, FILM COATED in 1 BLISTER PACK (67046-230-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67046-230The 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 NAMEGemfibrozilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/5/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEContract Pharmacy Services-PAName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/18/2019