55315-368 NDC - OMEPRAZOLE MAGNESIUM ()

Drug Information

Product NDC: 55315-368

Proprietary Name: Omeprazole Magnesium

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: FREDS
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/16/2015

Package Information

No. Package Code Package Description Billing Unit
155315-368-313 BOTTLE in 1 CARTON (55315-368-31) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC55315-368The 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 NAMEOmeprazole MagnesiumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/16/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFREDSName 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