Search by Drug Name or NDC

    NDC 71335-0863-07 Nitrofurantoin 25; 75 mg/1; mg/1 Details

    Nitrofurantoin 25; 75 mg/1; mg/1

    Nitrofurantoin is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE.

    Product Information

    NDC 71335-0863
    Product ID 71335-0863_caeadb30-df1d-43b3-b661-5354294102d4
    Associated GPIs 16800050150120
    GCN Sequence Number 016598
    GCN Sequence Number Description nitrofurantoin monohyd/m-cryst CAPSULE 100 MG ORAL
    HIC3 W2F
    HIC3 Description NITROFURAN DERIVATIVES ANTIBACTERIAL AGENTS
    GCN 49001
    HICL Sequence Number 006322
    HICL Sequence Number Description NITROFURANTOIN MONOHYDRATE/MACROCRYSTALS
    Brand/Generic Generic
    Proprietary Name Nitrofurantoin
    Proprietary Name Suffix (monohydrate/macrocrystals)
    Non-Proprietary Name Nitrofurantoin monohydrate/macrocrystals
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 25; 75
    Active Ingredient Units mg/1; mg/1
    Substance Name NITROFURANTOIN; NITROFURANTOIN MONOHYDRATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Nitrofuran Antibacterial [EPC], Nitrofuran Antibacterial [EPC], Nitrofurans [CS], Nitrofurans [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207372
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0863-07 (71335086307)

    NDC Package Code 71335-0863-7
    Billing NDC 71335086307
    Package 90 CAPSULE in 1 BOTTLE (71335-0863-7)
    Marketing Start Date 2018-12-07
    NDC Exclude Flag N
    Pricing Information N/A