Clinical Trials

Find trials by condition, location & phase

Drug Monographs

Browse drug monographs and information

Explore organizations and their profiles

Latest updates on trials and healthcare

Approved products by global authorities

AI-Powered Research

Discover powerful insights with advanced AI analysis tools for clinical trials.

Premium Access

Get unlimited access to our comprehensive pharmaceutical database and analytics.

FDA Approval

Integra F

Company

U.S. Pharmaceutical Corporation (DUNS: 079467662)

Effective Date

November 8, 2022

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Ferrous fumarate(62.5 mg in 1 1)

Vitamin C(40 mg in 1 1)

Niacin(3 mg in 1 1)

Ferrous asparto glycinate(62.5 mg in 1 1)

Folic acid(1 mg in 1 1)

Registrants (1)

U.S. Pharmaceutical Corporation

DUNS Number

079467662

Products (1)

Integra F

NDC Product Code

52747-711

Route of Administration

ORAL

Effective Date

July 13, 2022

Ingredients

Ferrous fumarateActive

Code: R5L488RY0QClass: ACTIMQuantity: 62.5 mg in 1 1

Vitamin CActive

Code: PQ6CK8PD0RClass: ACTIBQuantity: 40 mg in 1 1

NiacinActive

Code: 2679MF687AClass: ACTIBQuantity: 3 mg in 1 1

Ferrous asparto glycinateActive

Code: H7426RGB3LClass: ACTIMQuantity: 62.5 mg in 1 1

Folic acidActive

Code: 935E97BOY8Class: ACTIBQuantity: 1 mg in 1 1

HYPROMELLOSE, UNSPECIFIEDInactive

Code: 3NXW29V3WOClass: IACT

FD&C BLUE NO. 1Inactive

Code: H3R47K3TBDClass: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30Class: IACT

FD&C RED NO. 40Inactive

Code: WZB9127XOAClass: IACT

TITANIUM DIOXIDEInactive

Code: 15FIX9V2JPClass: IACT

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy