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  4. NDC Product Code: 59528-0416 Magnebind 400 Rx

NDC 59528-0416 Magnebind 400 Rx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59528-0416?
  5. Magnebind 400 Rx Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59528-0416
Proprietary Name:
Magnebind 400 Rx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nephro-tech, Inc.
Labeler Code:
59528
Product Label ID:
85044000-d313-4b3a-8b92-30e8e8e6dcc3
Start Marketing Date: [9]
10-18-1999
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
OVAL (C48345)
Size(s):
16 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 59528-0416?

The NDC code 59528-0416 is assigned by the FDA to the product Magnebind 400 Rx which is product labeled by Nephro-tech, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59528-0416-5 150 tablet, film coated in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Magnebind 400 Rx?

Patients who are hypermagnesemic or who have impaired renal function and are not being dialyzed should not be prescribed MagneBind 400 Rx.

Which are Magnebind 400 Rx UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Magnebind 400 Rx Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Magnebind 400 Rx?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 259567 - calcium 80 MG / folic acid 1 MG / magnesium 115 MG Oral Tablet
  • RxCUI: 259567 - calcium carbonate 200 MG / folic acid 1 MG / magnesium carbonate 400 MG Oral Tablet
  • RxCUI: 259567 - Calcium Carbonate 200 MG / folate 1 MG / magnesium carbonate 400 MG Oral Tablet
  • RxCUI: 794747 - MagneBind-400-Rx 115 MG / 80 MG / 1 MG Oral Tablet, as magnesium carbonate and calcium carbonate
  • RxCUI: 794747 - calcium carbonate 200 MG / folic acid 1 MG / magnesium carbonate 400 MG Oral Tablet [MagneBind 400 Rx]

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".