11819-371 NDC - ONDANSETRON ()

Drug Information

Product NDC: 11819-371

Proprietary Name: Ondansetron

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: United States Department of Health & Human Services
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/27/2014

Package Information

No. Package Code Package Description Billing Unit
111819-371-285 BLISTER PACK in 1 CARTON (11819-371-28) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (11819-371-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11819-371The 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 DATE10/27/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEUnited States Department of Health & Human ServicesName 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