17856-4091 NDC - ONDANSETRON ()

Drug Information

Product NDC: 17856-4091

Proprietary Name: Ondansetron

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Atlantic Biologicals Corps
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/17/2010

Package Information

No. Package Code Package Description Billing Unit
117856-4091-35 mL in 1 CUP (17856-4091-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC17856-4091The 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 NAMEOndansetronThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/17/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAtlantic Biologicals CorpsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/29/2020