Search by Drug Name or NDC

    NDC 80725-0712-04 AVODART 0.5 mg/1 Details

    AVODART 0.5 mg/1

    AVODART is a ORAL CAPSULE, LIQUID FILLED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Waylis Therapeutics LLC. The primary component is DUTASTERIDE.

    Product Information

    NDC 80725-0712
    Product ID 80725-712_ebeee383-e0e9-4524-a0b7-81a69c1cd2c5
    Associated GPIs
    GCN Sequence Number 051246
    GCN Sequence Number Description dutasteride CAPSULE 0.5 MG ORAL
    HIC3 Q9B
    HIC3 Description BENIGN PROSTATIC HYPERTROPHY/MICTURITION AGENTS
    GCN 18428
    HICL Sequence Number 024485
    HICL Sequence Number Description DUTASTERIDE
    Brand/Generic Brand
    Proprietary Name AVODART
    Proprietary Name Suffix n/a
    Non-Proprietary Name dutasteride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name DUTASTERIDE
    Labeler Name Waylis Therapeutics LLC
    Pharmaceutical Class 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021319
    Listing Certified Through 2024-12-31

    Package

    NDC 80725-0712-04 (80725071204)

    NDC Package Code 80725-712-04
    Billing NDC 80725071204
    Package 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (80725-712-04)
    Marketing Start Date 2022-12-15
    NDC Exclude Flag N
    Pricing Information N/A