59528-0416 NDC - MAGNEBIND 400 RX ()

Drug Information

Product NDC: 59528-0416

Proprietary Name: MagneBind 400 Rx

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Nephro-Tech, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/18/1999

Package Information

No. Package Code Package Description Billing Unit
159528-0416-5150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59528-0416-5)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC59528-0416The 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 NAMEMagneBind 400 RxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/18/1999This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENephro-Tech, Inc.Name 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