1. Home
  2. Labeler Index
  3. Nnodum Pharmaceuticals
  4. NDC Product Code: 63044-632 Hematogen Fa

NDC 63044-632 Hematogen Fa

View Dosage, Usage, Ingredients, Routes, UNII

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.

Get all the details for National Drug Code (NDC) 63044-632 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
63044-632
Proprietary Name:
Hematogen Fa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
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.
Start Marketing Date: [9]
01-01-2005
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
I
Code Navigator:

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 which is product labeled by Nnodum Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63044-632-17 10 blister pack in 1 box / 10 capsule in 1 blister pack. 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 Hematogen Fa?

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 Hematogen Fa UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Hematogen Fa?

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 disclaimer below.

Product Footnotes

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

[8] 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.

[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, 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".