NDC 63739-495

Finasteride

Finasteride

Finasteride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Mckesson Packaging Services Business Unit Of Mckesson Corporation. The primary component is Finasteride.

Product ID63739-495_da78d7ba-d9de-4b04-b088-640547ae1a98
NDC63739-495
Product TypeHuman Prescription Drug
Proprietary NameFinasteride
Generic NameFinasteride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-11-22
Marketing CategoryANDA / ANDA
Application NumberANDA077914
Labeler NameMcKesson Packaging Services Business Unit of McKesson Corporation
Substance NameFINASTERIDE
Active Ingredient Strength5 mg/1
Pharm Classes5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63739-495-43

90 TABLET, FILM COATED in 1 BOTTLE (63739-495-43)
Marketing Start Date2010-11-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63739-495-43 [63739049543]

Finasteride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077914
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-22
Inactivation Date2019-10-29

NDC 63739-495-41 [63739049541]

Finasteride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077914
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-22
Inactivation Date2019-10-29

NDC 63739-495-40 [63739049540]

Finasteride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077914
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-22
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
FINASTERIDE5 mg/1

OpenFDA Data

SPL SET ID:344a2e9e-24fa-4550-863e-ff56df0bf15c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310346
    • UPC Code
  • 0363739495418

    • Pharmacological Class

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

    NDC Crossover Matching brand name "Finasteride" or generic name "Finasteride"

    NDCBrand NameGeneric Name
    0093-7355FinasterideFinasteride
    0179-0175FinasterideFinasteride
    0378-5036Finasteridefinasteride
    0904-6830FinasterideFinasteride
    16729-089FinasterideFinasteride
    16729-090Finasteridefinasteride
    17856-0090Finasteridefinasteride
    31722-525FinasterideFinasteride
    31722-526FinasterideFinasteride
    33261-833FinasterideFinasteride
    35573-400FinasterideFinasteride
    42291-280FinasterideFinasteride
    43598-303FinasterideFinasteride
    43598-390FinasterideFinasteride
    45963-500FinasterideFinasteride
    45963-600FINASTERIDEFINASTERIDE
    47335-714FinasterideFinasteride
    47335-715FINASTERIDEFINASTERIDE
    50090-1718Finasteridefinasteride
    67877-288FinasterideFinasteride
    67877-455FinasterideFinasteride
    68071-1648FinasterideFinasteride
    68071-1710FinasterideFinasteride
    68071-3234FinasterideFinasteride
    68071-3306FinasterideFinasteride
    68071-4044FinasterideFinasteride
    68071-3354FinasterideFinasteride
    68071-3380FinasterideFinasteride
    68071-4167FinasterideFinasteride
    68071-4541FinasterideFinasteride
    68071-4808FinasterideFinasteride
    68084-399FinasterideFinasteride
    68382-074FinasterideFinasteride
    68645-541FinasterideFinasteride
    68554-3026FinasterideFinasteride
    68554-3025FinasterideFinasteride
    68788-6976FinasterideFinasteride
    68788-6875FinasterideFinasteride
    68788-9519FinasterideFinasteride
    68788-9249FinasterideFinasteride
    68788-9517FinasterideFinasteride
    69097-112FinasterideFinasteride
    70518-0397FinasterideFinasteride
    70518-1704FinasterideFinasteride
    70771-1152FinasterideFinasteride
    71335-0433FinasterideFinasteride
    71335-0281FinasterideFinasteride
    71335-0235FinasterideFinasteride
    76282-412FinasterideFinasteride
    76519-1204FINASTERIDEFINASTERIDE
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