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  5. NDC Package Code: 52747-711-30 Integra F

NDC Package 52747-711-30 Integra F

Ferrous Fumarate And Polysacchride Iron Complex And Folic Acid Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
52747-711-30
Package Description:
30 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
52747-711
Proprietary Name:
Integra F
Non-Proprietary Name:
Ferrous Fumarate And Polysacchride Iron Complex And Folic Acid
Substance Name:
Ascorbic Acid; Ferrous Asparto Glycinate; Ferrous Fumarate; Folic Acid; Niacin
Usage Information:
INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid.
11-Digit NDC Billing Format:
52747071130
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 999823 - ascorbic acid 40 MG / ferrous fumarate 191 MG / folic acid 1 MG / niacinamide 3 MG / polysaccharide iron complex 136 MG Oral Capsule
  • RxCUI: 999823 - vitamin C 40 MG / Ferrous fumarate 191 MG / folate 1 MG / Niacinamide 3 MG / Polysaccharide iron complex 136 MG Oral Capsule
  • RxCUI: 999823 - vit-C 40 MG / Ferrous fumarate 191 MG / folate 1 MG / Niacinamide 3 MG / Polysaccharide iron complex 136 MG Oral Capsule
  • RxCUI: 999826 - ascorbic acid 40 MG / ferrous fumarate 191 MG / folic acid 1 MG / niacinamide 3 MG / polysaccharide iron complex 136 MG Oral Capsule [Integra F]
  • RxCUI: 999826 - Integra F (ascorbic acid 40 MG / ferrous fumarate 191 MG (iron 62.5 MG) / folic acid 1 MG / vitamin B3 3 MG / polysaccharide iron complex 136 MG (iron 62.5 MG)) Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    U.s. Pharmaceutical Corporation
    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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ASCORBIC ACID 40 mg/1
  • FERROUS ASPARTO GLYCINATE 62.5 mg/1
  • FERROUS FUMARATE 62.5 mg/1
  • FOLIC ACID 1 mg/1
  • NIACIN 3 mg/1
    • Pharmacologic Class(es):
  • Ascorbic Acid - [CS]
  • Nicotinic Acid - [EPC] (Established Pharmacologic Class)
  • Nicotinic Acids - [CS]
  • Vitamin C - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    04-27-2009
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    52747-711-6090 CAPSULE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52747-711-30?

    The NDC Packaged Code 52747-711-30 is assigned to a package of 30 capsule in 1 bottle, plastic of Integra F, a human prescription drug labeled by U.s. Pharmaceutical Corporation. The product's dosage form is capsule and is administered via oral form.

    Is NDC 52747-711 included in the NDC Directory?

    Yes, Integra F with product code 52747-711 is active and included in the NDC Directory. The product was first marketed by U.s. Pharmaceutical Corporation on April 27, 2009 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 52747-711-30?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 52747-711-30?

    The 11-digit format is 52747071130. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-252747-711-305-4-252747-0711-30