NDC 0173-0712

AVODART

Dutasteride

AVODART is a Oral Capsule, Liquid Filled in the Human Prescription Drug category. It is labeled and distributed by Glaxosmithkline Llc. The primary component is Dutasteride.

Product ID0173-0712_0a9894f0-06bc-4e0e-a74b-5df75d9786a8
NDC0173-0712
Product TypeHuman Prescription Drug
Proprietary NameAVODART
Generic NameDutasteride
Dosage FormCapsule, Liquid Filled
Route of AdministrationORAL
Marketing Start Date2002-12-10
Marketing CategoryNDA / NDA
Application NumberNDA021319
Labeler NameGlaxoSmithKline LLC
Substance NameDUTASTERIDE
Active Ingredient Strength1 mg/1
Pharm Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0173-0712-04

90 CAPSULE, LIQUID FILLED in 1 BOTTLE (0173-0712-04)
Marketing Start Date2002-12-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0173-0712-04 [00173071204]

AVODART CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021319
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-12-10

NDC 0173-0712-15 [00173071215]

AVODART CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021319
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-12-10

NDC 0173-0712-02 [00173071202]

AVODART CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021319
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-12-10
Marketing End Date2018-04-30

NDC 0173-0712-25 [00173071225]

AVODART CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021319
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-07-31
Marketing End Date2013-04-08

Drug Details

Active Ingredients

IngredientStrength
DUTASTERIDE.5 mg/1

OpenFDA Data

SPL SET ID:dc330e70-a1d3-400b-3aaf-46067e3fd090
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351172
  • 352118
    • UPC Code
  • 0301730712042

    • Pharmacological Class

    • 5-alpha Reductase Inhibitor [EPC]
    • 5-alpha Reductase Inhibitors [MoA]

    NDC Crossover Matching brand name "AVODART" or generic name "Dutasteride"

    NDCBrand NameGeneric Name
    0173-0712AVODARTdutasteride
    0054-0395DutasterideDutasteride
    0115-1438DutasterideDutasteride
    0591-2292DutasterideDutasteride
    25000-011DutasterideDutasteride
    31722-131DutasterideDutasteride
    42543-139DutasterideDutasteride
    42806-549DutasterideDutasteride
    50090-2285Dutasteridedutasteride
    50090-3040DutasterideDutasteride
    50090-4010DutasterideDutasteride
    50268-282DutasterideDutasteride
    51013-190DutasterideDutasteride
    51407-157DutasterideDutasteride
    51991-749DUTASTERIDEDUTASTERIDE
    53345-037DutasterideDutasteride
    60429-935Dutasteridedutasteride
    60505-3877Dutasteridedutasteride
    62112-8068Dutasteridedutasteride
    63187-657DutasterideDutasteride
    63629-1222DutasterideDutasteride
    63629-1223DutasterideDutasteride
    63629-8207DutasterideDutasteride
    64380-763DutasterideDutasteride
    64980-224DUTASTERIDEdutasteride

    Trademark Results [AVODART]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    AVODART
    AVODART
    78160900 2891877 Dead/Cancelled
    SMITHKLINE BEECHAM CORPORATION
    2002-09-05
    AVODART
    AVODART
    78089208 2854915 Live/Registered
    GLAXOSMITHKLINE LLC
    2001-10-19
    AVODART
    AVODART
    77020399 3328344 Dead/Cancelled
    SmithKline Beecham Corporation
    2006-10-13
    AVODART
    AVODART
    75804768 2364700 Dead/Cancelled
    SMITHKLINE BEECHAM CORPORATION
    1999-09-17
    AVODART
    AVODART
    75218090 not registered Dead/Abandoned
    SmithKline Beecham P.L.C.
    1996-12-20
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