Hematogen Fa
NDC 63044-632

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63044-632?
  5. Hematogen Fa Uses
  6. Active Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Hematogen Fa is a UNAPPROVED DRUG OTHER-approved product labeled by Nnodum Pharmaceuticals. This combination product contains a mineral (iron) along with 3 vitamins (vitamin C, vitamin B12, and folic acid). It is supplied as a brown product. This product entry covers the primary NDC 63044-632 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
63044-632
Proprietary Name:
Hematogen Fa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Nnodum Pharmaceuticals
Labeler Code:
63044
Product Label ID:
fa1db7ce-a733-4036-aa4b-c4aec29829c1
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
01-01-2005
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
I

Product Characteristics

Color(s):
BROWN (C48332 - MAROON;BROWN)
Shape:
CAPSULE (C48336)
Size(s):
1 MM
Imprint(s):
NONE
Score:
1

Code Structure Chart

Product Details

What is NDC 63044-632?

The NDC code 63044-632 is assigned by the FDA to the product Hematogen Fa. This pharmaceutical product is labeled by Nnodum Pharmaceuticals and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63044-632-17. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

This combination product contains a mineral (iron) along with 3 vitamins (vitamin C, vitamin B12, and folic acid). It is used to treat or prevent a lack of these nutrients which may occur in certain health conditions (e.g., anemia, pregnancy, poor diet, surgery recovery). Iron is an important mineral that the body needs to produce red blood cells. Vitamin C improves the absorption of iron from the stomach. Vitamin B12 is important for normal blood, cells, and nerves. Folic acid is needed to form healthy cells, especially red blood cells. Women of childbearing age should maintain adequate amounts of folic acid either through diet or supplements to prevent spinal cord birth defects.

Which are the associated UNII Codes?

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

What is the NDC to RxNorm Crosswalk for this product?

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: 348622 - ascorbic acid 250 MG / ferrous fumarate 200 MG / folic acid 1 MG / vitamin B12 0.01 MG Oral Capsule
  • RxCUI: 348622 - ascorbic acid 250 MG / cyanocobalamin 10 MCG / ferrous fumarate 200 MG / folic acid 1 MG Oral Capsule
  • RxCUI: 348622 - vitamin C 250 MG / ferrous fumarate 200 MG / folate 1 MG / vitamin B12 0.01 MG Oral Capsule
  • RxCUI: 348622 - vit-C 250 MG / ferrous fumarate 200 MG / folate 1 MG / vitamin B12 0.01 MG Oral Capsule
  • RxCUI: 999749 - ascorbic acid 250 MG / ferrous fumarate 200 MG / folic acid 1 MG / vitamin B12 0.01 MG Oral Capsule [Hematogen]

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".