68233-810 NDC - AA TOP MEDICATED ()

Drug Information

Product NDC: 68233-810

Proprietary Name: AA Top Medicated

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Albert Max, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2018

Package Information

No. Package Code Package Description Billing Unit
168233-810-0150 mL in 1 BOTTLE (68233-810-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68233-810The 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 NAMEAA Top MedicatedThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAlbert Max, Inc.Name 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