53002-0570 NDC - ONDANSETRON ()

Drug Information

Product NDC: 53002-0570

Proprietary Name: Ondansetron

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RPK Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/27/2007

Package Information

No. Package Code Package Description Billing Unit
153002-0570-13 TABLET, FILM COATED in 1 BOTTLE (53002-0570-1)
253002-0570-26 TABLET, FILM COATED in 1 BOTTLE (53002-0570-2)
353002-0570-310 TABLET, FILM COATED in 1 BOTTLE (53002-0570-3)
453002-0570-430 TABLET, FILM COATED in 1 BOTTLE (53002-0570-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53002-0570The 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 DATE7/27/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERPK Pharmaceuticals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023