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  4. NDC Product Code: 44523-732 Bioferr 90

NDC 44523-732 Bioferr 90

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 44523-732?
  5. Bioferr 90 Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44523-732
Proprietary Name:
Bioferr 90
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biocomp Pharma, Inc.
Labeler Code:
44523
Product Label ID:
878e22cc-9f69-3074-3212-2b36763b2a65
Start Marketing Date: [9]
07-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
RECTANGLE (C48347)
Size(s):
9 MM
Imprint(s):
F7
Score:
1

Product Packages

NDC Code 44523-732-90

Package Description: 90 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 44523-732?

The NDC code 44523-732 is assigned by the FDA to the product Bioferr 90 which is product labeled by Biocomp Pharma, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44523-732-90 90 tablet, film coated in 1 bottle . 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 Bioferr 90?

BioFerr™ 90 is indicated for the treatment of all anemias that are responsive to oral iron therapy. These include: hypochromic anemia associated with pregnancy, chronic and/or acute blood loss, metabolic disease, post-surgical convalescence, and dietary needs.

Which are Bioferr 90 UNII Codes?

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

Which are Bioferr 90 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:

* 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".