52083-625 NDC - ABATUSS DMX ()

Drug Information

Product NDC: 52083-625

Proprietary Name: ABATUSS DMX

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Kramer Novis
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/25/2014

Package Information

No. Package Code Package Description Billing Unit
152083-625-161 BOTTLE in 1 CARTON (52083-625-16) / 473 mL in 1 BOTTLEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC52083-625The 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 NAMEABATUSS DMXThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/25/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKramer NovisName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024