51655-415 NDC - ONDANSETRON HYDROCHLORIDE ()

Drug Information

Product NDC: 51655-415

Proprietary Name: Ondansetron Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Northwind Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/7/2017

Package Information

No. Package Code Package Description Billing Unit
151655-415-044 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)
251655-415-433 TABLET, FILM COATED in 1 BOTTLE (51655-415-43)
351655-415-5310 TABLET, FILM COATED in 1 BOTTLE (51655-415-53)
451655-415-5415 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)
551655-415-555 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)
651655-415-876 TABLET, FILM COATED in 1 BOTTLE (51655-415-87)

NDC Record

Field Name Field Value Definition
PRODUCT NDC51655-415The 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 NAMEOndansetron HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/7/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENorthwind PharmaceuticalsName 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