13107-117 NDC - OMEPRAZOLE AND SODIUM BICARBONATE ()

Drug Information

Product NDC: 13107-117

Proprietary Name: Omeprazole and Sodium Bicarbonate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aurolife Pharma, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/30/2014

Package Information

No. Package Code Package Description Billing Unit
113107-117-141 BOTTLE in 1 CARTON (13107-117-14) / 14 CAPSULE in 1 BOTTLE
213107-117-282 BOTTLE in 1 CARTON (13107-117-28) / 14 CAPSULE in 1 BOTTLE
313107-117-423 BOTTLE in 1 CARTON (13107-117-42) / 14 CAPSULE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC13107-117The 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 and Sodium BicarbonateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAurolife Pharma, LLCName 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