75854-321 NDC - NIFEREX (FERROUS ASPARTO GLYCINATE, IRON, ASCORBIC ACID, FOLIC ACID, CYANOCOBALAMIN, ZINC, SUCCINIC ACID, AND INTRINSIC FACTOR)

Drug Information

Product NDC: 75854-321

Proprietary Name: Niferex

Non Proprietary Name: ferrous asparto glycinate, iron, ascorbic acid, folic acid, cyanocobalamin, zinc, succinic acid, and intrinsic factor

Active Ingredient(s):
  • 60 mg/1 ASCORBIC ACID;
  • 25 ug/1 CYANOCOBALAMIN;
  • 50 mg/1 FERROUS ASPARTO GLYCINATE;
  • 250 ug/1 FOLIC ACID;
  • 100 mg/1 INTRINSIC FACTOR;
  • 100 mg/1 IRON DEXTRAN;
  • 750 ug/1 LEVOMEFOLIC ACID;
  • 50 mg/1 SUCCINIC ACID;
  • 15 mg/1 ZINC


Administration Route(s): ORAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Ascorbic Acid [CS];
  • Iron [CS];
  • Parenteral Iron Replacement [EPC];
  • Phosphate Binder [EPC];
  • Phosphate Chelating Activity [MoA];
  • Vitamin B 12 [CS];
  • Vitamin B12 [EPC];
  • Vitamin C [EPC]

Labeler Information

Labeler Name: Avion Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:1/10/2017

Package Information

No. Package Code Package Description Billing Unit
175854-321-3030 TABLET in 1 BOTTLE (75854-321-30)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC75854-321The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMENiferexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEferrous asparto glycinate, iron, ascorbic acid, folic acid, cyanocobalamin, zinc, succinic acid, and intrinsic factorThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/10/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEAvion Pharmaceuticals, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEASCORBIC ACID; CYANOCOBALAMIN; FERROUS ASPARTO GLYCINATE; FOLIC ACID; INTRINSIC FACTOR; IRON DEXTRAN; LEVOMEFOLIC ACID; SUCCINIC ACID; ZINCAn 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.
ACTIVE NUMERATOR STRENGTH60; 25; 50; 250; 100; 100; 750; 50; 15 
ACTIVE INGRED UNITmg/1; ug/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1 
PHARM CLASSESAscorbic Acid [CS], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Vitamin B 12 [CS], Vitamin B12 [EPC], Vitamin C [EPC] 

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This page was last updated on: 2/1/2023