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    NDC 52747-0711-60 Integra F 40; 62.5; 62.5; 1; 3 mg/1; mg/1; mg/1; mg/1; mg/1 Details

    Integra F 40; 62.5; 62.5; 1; 3 mg/1; mg/1; mg/1; mg/1; mg/1

    Integra F is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by U.S. Pharmaceutical Corporation. The primary component is ASCORBIC ACID; FERROUS ASPARTO GLYCINATE; FERROUS FUMARATE; FOLIC ACID; NIACIN.

    Product Information

    NDC 52747-0711
    Product ID 52747-711_7aa8c3c6-7a91-4217-9e48-e1dfcf938060
    Associated GPIs 82994005600130
    GCN Sequence Number 065099
    GCN Sequence Number Description iron fum,ps/folic acid/vitC/B3 CAPSULE 125-1-40-3 ORAL
    HIC3 C3B
    HIC3 Description IRON REPLACEMENT
    GCN 22177
    HICL Sequence Number 036268
    HICL Sequence Number Description IRON FUMARATE,POLYSAC COMP/FOLIC ACID/VITAMIN C/NIACINAMIDE
    Brand/Generic Brand
    Proprietary Name Integra F
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 40; 62.5; 62.5; 1; 3
    Active Ingredient Units mg/1; mg/1; mg/1; mg/1; mg/1
    Substance Name ASCORBIC ACID; FERROUS ASPARTO GLYCINATE; FERROUS FUMARATE; FOLIC ACID; NIACIN
    Labeler Name U.S. Pharmaceutical Corporation
    Pharmaceutical Class Ascorbic Acid [CS], Nicotinic Acid [EPC], Nicotinic Acids [CS], Vitamin C [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 52747-0711-60 (52747071160)

    NDC Package Code 52747-711-60
    Billing NDC 52747071160
    Package 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-60)
    Marketing Start Date 2009-04-27
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 025fee85-53a8-4161-a806-44fd95d0ca74 Details

    Revised: 11/2022