NDC 0002-3240

Cymbalta

Duloxetine Hydrochloride

Cymbalta is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Eli Lilly And Company. The primary component is Duloxetine Hydrochloride.

Product ID0002-3240_06e2a1f2-459c-45aa-9341-54e36f7726a7
NDC0002-3240
Product TypeHuman Prescription Drug
Proprietary NameCymbalta
Generic NameDuloxetine Hydrochloride
Dosage FormCapsule, Delayed Release
Route of AdministrationORAL
Marketing Start Date2004-08-24
Marketing CategoryNDA / NDA
Application NumberNDA021427
Labeler NameEli Lilly and Company
Substance NameDULOXETINE HYDROCHLORIDE
Active Ingredient Strength30 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0002-3240-30

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30)
Marketing Start Date2004-08-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0002-3240-90 [00002324090]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-08-24

NDC 0002-3240-33 [00002324033]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-08-24
Marketing End Date2016-08-31

NDC 0002-3240-30 [00002324030]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-08-24

NDC 0002-3240-01 [00002324001]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-08-24
Marketing End Date2019-04-17

NDC 0002-3240-07 [00002324007]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-08-24
Marketing End Date2015-12-31

NDC 0002-3240-04 [00002324004]

Cymbalta CAPSULE, DELAYED RELEASE
Marketing CategoryNDA
Application NumberNDA021427
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-08-24
Marketing End Date2012-09-13

Drug Details

Active Ingredients

IngredientStrength
DULOXETINE HYDROCHLORIDE30 mg/1

OpenFDA Data

SPL SET ID:2f7d4d67-10c1-4bf4-a7f2-c185fbad64ba
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 615186
  • 596932
  • 596930
  • 596934
  • 596926
  • 596928
    • UPC Code
  • 0300023240309

    • Pharmacological Class

    • Norepinephrine Uptake Inhibitors [MoA]
    • Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Cymbalta" or generic name "Duloxetine Hydrochloride"

    NDCBrand NameGeneric Name
    0002-3235CymbaltaDuloxetine hydrochloride
    0002-3240CymbaltaDuloxetine hydrochloride
    0002-3270CymbaltaDuloxetine hydrochloride
    21695-145CymbaltaDuloxetine hydrochloride
    21695-146CymbaltaDuloxetine hydrochloride
    68151-4734CymbaltaCymbalta
    68151-4679CymbaltaCymbalta
    21695-657CymbaltaCymbalta
    35356-843CymbaltaCymbalta
    43353-303CymbaltaCymbalta
    49999-618CymbaltaCymbalta
    52959-892CymbaltaCymbalta
    55289-028CymbaltaCymbalta
    55289-036CymbaltaCymbalta
    70518-2100CymbaltaCymbalta
    70518-2099CymbaltaCymbalta
    80425-0086CymbaltaCymbalta
    80425-0119CymbaltaCymbalta
    0904-7043DuloxetineDuloxetine Hydrochloride
    0904-7044DuloxetineDuloxetine Hydrochloride
    0904-7045DuloxetineDuloxetine Hydrochloride
    0615-8034Duloxetine HydrochlorideDuloxetine Hydrochloride
    0615-8035Duloxetine HydrochlorideDuloxetine Hydrochloride
    0904-6452Duloxetine HydrochlorideDuloxetine Hydrochloride
    0904-6453Duloxetine HydrochlorideDuloxetine Hydrochloride
    0904-6454Duloxetine HydrochlorideDuloxetine Hydrochloride

    Trademark Results [Cymbalta]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CYMBALTA
    CYMBALTA
    78859969 3194152 Live/Registered
    Eli Lilly and Company
    2006-04-12
    CYMBALTA
    CYMBALTA
    76535580 not registered Dead/Abandoned
    Eli Lilly and Company
    2003-07-25
    CYMBALTA
    CYMBALTA
    75867543 2802665 Live/Registered
    Eli Lilly and Company
    1999-12-09
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