44224-3621 NDC - AFTER BITE WIPE ()

Drug Information

Product NDC: 44224-3621

Proprietary Name: After Bite Wipe

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Tender Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2016

Package Information

No. Package Code Package Description Billing Unit
144224-3621-01.1 mL in 1 POUCH (44224-3621-0)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44224-3621The 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 NAMEAfter Bite WipeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETender 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