21695-232 NDC - NAMENDA ()

Drug Information

Product NDC: 21695-232

Proprietary Name: Namenda

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rebel Distributors Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/9/2006

Package Information

No. Package Code Package Description Billing Unit
121695-232-6060 TABLET in 1 BOTTLE (21695-232-60)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC21695-232The 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 NAMENamendaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/9/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERebel Distributors CorpName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/26/2021