NDC 63044-632 Hematogen Fa

Ferrous Fumarate,Ascorbic Acid,Folic Acid,Cyanocobalamin Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
63044-632
Proprietary Name:
Hematogen Fa
Non-Proprietary Name: [1]
Ferrous Fumarate, Ascorbic Acid, Folic Acid, Cyanocobalamin
Substance Name: [2]
Ascorbic Acid; Cyanocobalamin; Ferrous Fumarate; Folic Acid
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Nnodum Pharmaceuticals
    Labeler Code:
    63044
    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]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

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

    Product Packages

    NDC Code 63044-632-17

    Package Description: 10 BLISTER PACK in 1 BOX / 10 CAPSULE in 1 BLISTER PACK

    Product Details

    What is NDC 63044-632?

    The NDC code 63044-632 is assigned by the FDA to the product Hematogen Fa which is a human prescription drug product labeled by Nnodum Pharmaceuticals. The generic name of Hematogen Fa is ferrous fumarate, ascorbic acid, folic acid, cyanocobalamin. The product's dosage form is capsule and is administered via oral form. 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.

    What are Hematogen Fa Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • ASCORBIC ACID 250 mg/1 - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
    • CYANOCOBALAMIN 10 ug/1
    • FERROUS FUMARATE 66 mg/1
    • FOLIC ACID 1 mg/1 - A member of the vitamin B family that stimulates the hematopoietic system. It is present in the liver and kidney and is found in mushrooms, spinach, yeast, green leaves, and grasses (POACEAE). Folic acid is used in the treatment and prevention of folate deficiencies and megaloblastic anemia.

    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]

    Which are the Pharmacologic Classes for Hematogen Fa?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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 ("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".