NDC 63402-304

Latuda

Lurasidone Hydrochloride

Latuda is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sunovion Pharmaceuticals Inc.. The primary component is Lurasidone Hydrochloride.

Product ID63402-304_659f4f38-e487-4e67-bc2e-d97f617c67c1
NDC63402-304
Product TypeHuman Prescription Drug
Proprietary NameLatuda
Generic NameLurasidone Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-10-28
Marketing CategoryNDA / NDA
Application NumberNDA200603
Labeler NameSunovion Pharmaceuticals Inc.
Substance NameLURASIDONE HYDROCHLORIDE
Active Ingredient Strength40 mg/1
Pharm ClassesAtypical Antipsychotic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63402-304-04

4 BLISTER PACK in 1 CARTON (63402-304-04) > 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-07)
Marketing Start Date2010-10-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63402-304-07 [63402030407]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-28

NDC 63402-304-01 [63402030401]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-10-28

NDC 63402-304-04 [63402030404]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-28

NDC 63402-304-30 [63402030430]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-10-28

NDC 63402-304-10 [63402030410]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-10-28

NDC 63402-304-50 [63402030450]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-28

NDC 63402-304-90 [63402030490]

Latuda TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA200603
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-28

Drug Details

Active Ingredients

IngredientStrength
LURASIDONE HYDROCHLORIDE40 mg/1

OpenFDA Data

SPL SET ID:afad3051-9df2-4c54-9684-e8262a133af8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1040031
  • 1040036
  • 1297357
  • 1040041
  • 1297278
  • 1431235
  • 1431237
  • 1235249
  • 1235247
  • 1040043
    • UPC Code
  • 0363402306904
  • 0363402306300
  • 0363402304306
  • 0363402312301
  • 0363402306102
  • 0363402306508
  • 0363402302302
  • 0363402308304

    • Pharmacological Class

    • Atypical Antipsychotic [EPC]

    Medicade Reported Pricing

    63402030430 LATUDA 40 MG TABLET

    Pricing Unit: EA | Drug Type:

    63402030410 LATUDA 40 MG TABLET

    Pricing Unit: EA | Drug Type:

    63402030401 LATUDA 40 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Latuda" or generic name "Lurasidone Hydrochloride"

    NDCBrand NameGeneric Name
    63402-302Latudalurasidone hydrochloride
    63402-304Latudalurasidone hydrochloride
    63402-306Latudalurasidone hydrochloride
    63402-308Latudalurasidone hydrochloride
    63402-312Latudalurasidone hydrochloride
    70518-1812Latudalurasidone hydrochloride
    70518-1824LatudaLatuda
    70518-1936LatudaLatuda
    70518-3010LatudaLatuda
    13668-464Lurasidone HydrochlorideLurasidone Hydrochloride
    13668-465Lurasidone HydrochlorideLurasidone Hydrochloride
    13668-466Lurasidone HydrochlorideLurasidone Hydrochloride
    13668-467Lurasidone HydrochlorideLurasidone Hydrochloride
    46708-494Lurasidone HydrochlorideLurasidone Hydrochloride
    46708-495Lurasidone HydrochlorideLurasidone Hydrochloride
    46708-496Lurasidone HydrochlorideLurasidone Hydrochloride
    46708-497Lurasidone HydrochlorideLurasidone Hydrochloride
    46708-498Lurasidone HydrochlorideLurasidone Hydrochloride
    62332-494Lurasidone HydrochlorideLurasidone Hydrochloride
    62332-495Lurasidone HydrochlorideLurasidone Hydrochloride
    62332-496Lurasidone HydrochlorideLurasidone Hydrochloride
    62332-497Lurasidone HydrochlorideLurasidone Hydrochloride
    62332-498Lurasidone HydrochlorideLurasidone Hydrochloride
    65162-082Lurasidone HydrochlorideLurasidone Hydrochloride
    65162-879Lurasidone HydrochlorideLurasidone Hydrochloride
    65162-880Lurasidone HydrochlorideLurasidone Hydrochloride
    65162-881Lurasidone HydrochlorideLurasidone Hydrochloride
    65162-882Lurasidone HydrochlorideLurasidone Hydrochloride
    67877-638lurasidone hydrochloridelurasidone hydrochloride
    67877-639lurasidone hydrochloridelurasidone hydrochloride
    67877-640lurasidone hydrochloridelurasidone hydrochloride
    67877-641lurasidone hydrochloridelurasidone hydrochloride
    67877-642lurasidone hydrochloridelurasidone hydrochloride

    Trademark Results [Latuda]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LATUDA
    LATUDA
    77680062 3708035 Live/Registered
    SUMITOMO DAINIPPON PHARMA CO., LTD.
    2009-02-27
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