70934-118 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 70934-118

Proprietary Name: Omeprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/11/2018

Package Information

No. Package Code Package Description Billing Unit
170934-118-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-118-30)EA
270934-118-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-118-60)EA
370934-118-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-118-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC70934-118The 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 NAMEOmeprazoleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/11/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDenton Pharma, Inc. DBA Northwind PharmaceuticalsName 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