11822-5211 NDC - RITE AID ()

Drug Information

Product NDC: 11822-5211

Proprietary Name: Rite Aid

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:5/1/2016

Package Information

No. Package Code Package Description Billing Unit
111822-5211-685 g in 1 TUBE (11822-5211-6)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-5211The 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 NAMERite AidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2016A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
LABELER NAMERite Aid CorporationThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

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This page was last updated on: 2/1/2023