11822-0915 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 11822-0915

Proprietary Name: omeprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rite Aid Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/25/2008

Package Information

No. Package Code Package Description Billing Unit
111822-0915-12 CARTON in 1 CARTON (11822-0915-1) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
211822-0915-214 BLISTER PACK in 1 CARTON (11822-0915-2) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
311822-0915-33 CARTON in 1 CARTON (11822-0915-3) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
411822-0915-42 BOTTLE in 1 CARTON (11822-0915-4) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
511822-0915-51 BOTTLE in 1 CARTON (11822-0915-5) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
611822-0915-63 BOTTLE in 1 CARTON (11822-0915-6) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-0915The 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 DATE2/25/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERite Aid CorporationName 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