Search by Drug Name or NDC

    NDC 68382-0058-01 Warfarin Sodium 7.5 mg/1 Details

    Warfarin Sodium 7.5 mg/1

    Warfarin Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is WARFARIN SODIUM.

    Product Information

    NDC 68382-0058
    Product ID 68382-058_5bff866a-04d9-4326-83d3-4e9607b2e860
    Associated GPIs 83200030200320
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Warfarin Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Warfarin Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 7.5
    Active Ingredient Units mg/1
    Substance Name WARFARIN SODIUM
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Vitamin K Antagonist [EPC], Vitamin K Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040663
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0058-01 (68382005801)

    NDC Package Code 68382-058-01
    Billing NDC 68382005801
    Package 100 TABLET in 1 BOTTLE (68382-058-01)
    Marketing Start Date 2006-06-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e9d8fb69-a4c7-48cb-a4a9-e5d18eb4fd63 Details

    Revised: 11/2022