NDC 63044-632 Hematogen Fa
Ferrous Fumarate,Ascorbic Acid,Folic Acid,Cyanocobalamin Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63044 - Nnodum Pharmaceuticals
- 63044-632 - Hematogen Fa
Product Characteristics
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?
What are the uses for Hematogen Fa?
What are Hematogen Fa Active Ingredients?
- 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:
- FERROUS FUMARATE (UNII: R5L488RY0Q)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Hematogen Fa?
- 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?
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[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".