Search Icon

52959-643 NDC - TOPIRAMATE ()

Drug Information

Product NDC: 52959-643

Proprietary Name: TOPIRAMATE

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: H.J. Harkins Company, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/27/2009

Package Information

No. Package Code Package Description Billing Unit
152959-643-3030 TABLET, FILM COATED in 1 BOTTLE (52959-643-30)EA
252959-643-6060 TABLET, FILM COATED in 1 BOTTLE (52959-643-60)EA
352959-643-9090 TABLET, FILM COATED in 1 BOTTLE (52959-643-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52959-643The 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 NAMETOPIRAMATEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/27/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEH.J. Harkins Company, 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