72898-001 NDC - DAB ()

Drug Information

Product NDC: 72898-001

Proprietary Name: DAB

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Three Kings Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/10/2020

Package Information

No. Package Code Package Description Billing Unit
172898-001-0145 mL in 1 BOTTLE, PUMP (72898-001-01)
272898-001-02250 mL in 1 BOTTLE, PUMP (72898-001-02)
372898-001-031200 mL in 1 BOTTLE, PUMP (72898-001-03)
472898-001-04946352 mL in 1 DRUM (72898-001-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72898-001The 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 NAMEDABThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/10/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEThree Kings CorpName 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