Search by Drug Name or NDC

    NDC 68382-0722-01 Nateglinide 120 mg/1 Details

    Nateglinide 120 mg/1

    Nateglinide is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is NATEGLINIDE.

    Product Information

    NDC 68382-0722
    Product ID 68382-722_061a2260-2804-4753-b443-17943eca74dd
    Associated GPIs 27280040000330
    GCN Sequence Number 047292
    GCN Sequence Number Description nateglinide TABLET 120 MG ORAL
    HIC3 C4K
    HIC3 Description ANTIHYPERGLYCEMIC, INSULIN-RELEASE STIMULANT TYPE
    GCN 34027
    HICL Sequence Number 021859
    HICL Sequence Number Description NATEGLINIDE
    Brand/Generic Generic
    Proprietary Name Nateglinide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Nateglinide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 120
    Active Ingredient Units mg/1
    Substance Name NATEGLINIDE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Glinide [EPC], Potassium Channel Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205248
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0722-01 (68382072201)

    NDC Package Code 68382-722-01
    Billing NDC 68382072201
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68382-722-01)
    Marketing Start Date 2016-10-27
    NDC Exclude Flag N
    Pricing Information N/A