NDC 0078-0324

Exelon

Rivastigmine Tartrate

Exelon is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is Rivastigmine Tartrate.

Product ID0078-0324_cb8c7caf-a61a-48a7-933d-4720ee22cdbc
NDC0078-0324
Product TypeHuman Prescription Drug
Proprietary NameExelon
Generic NameRivastigmine Tartrate
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2000-04-30
Marketing CategoryNDA / NDA
Application NumberNDA020823
Labeler NameNovartis Pharmaceuticals Corporation
Substance NameRIVASTIGMINE TARTRATE
Active Ingredient Strength3 mg/1
Pharm ClassesCholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0078-0324-15

30 CAPSULE in 1 BLISTER PACK (0078-0324-15)
Marketing Start Date2000-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0078-0324-61 [00078032461]

Exelon CAPSULE
Marketing CategoryNDA
Application NumberNDA020823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-04-13

NDC 0078-0324-06 [00078032406]

Exelon CAPSULE
Marketing CategoryNDA
Application NumberNDA020823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-04-30
Marketing End Date2012-06-30

NDC 0078-0324-15 [00078032415]

Exelon CAPSULE
Marketing CategoryNDA
Application NumberNDA020823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2000-04-30

NDC 0078-0324-44 [00078032444]

Exelon CAPSULE
Marketing CategoryNDA
Application NumberNDA020823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-04-30
Marketing End Date2017-06-30

NDC 0078-0324-08 [00078032408]

Exelon CAPSULE
Marketing CategoryNDA
Application NumberNDA020823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2000-04-30

Drug Details

Active Ingredients

IngredientStrength
RIVASTIGMINE TARTRATE3 mg/1

OpenFDA Data

SPL SET ID:f1e28b44-3897-4788-9659-f5d6bce4d91e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314214
  • 226668
  • 226665
  • 226666
  • 226667
  • 312835
  • 312836
  • 314215

    • Pharmacological Class

    • Cholinesterase Inhibitor [EPC]
    • Cholinesterase Inhibitors [MoA]
    • Cholinesterase Inhibitor [EPC]
    • Cholinesterase Inhibitors [MoA]

    NDC Crossover Matching brand name "Exelon" or generic name "Rivastigmine Tartrate"

    NDCBrand NameGeneric Name
    0078-0323Exelonrivastigmine tartrate
    0078-0324Exelonrivastigmine tartrate
    0078-0325Exelonrivastigmine tartrate
    0078-0326Exelonrivastigmine tartrate
    0078-0501Exelonrivastigmine
    0078-0502Exelonrivastigmine
    0078-0503Exelonrivastigmine
    21695-357Exelonrivastigmine
    0591-3208Rivastigmine TartrateRivastigmine Tartrate
    0591-3209Rivastigmine TartrateRivastigmine Tartrate
    0591-3210Rivastigmine TartrateRivastigmine Tartrate
    0591-3211Rivastigmine TartrateRivastigmine Tartrate
    0781-2614Rivastigmine Tartraterivastigmine tartrate
    0781-2615Rivastigmine Tartraterivastigmine tartrate
    0781-2616Rivastigmine Tartraterivastigmine tartrate
    0781-2617Rivastigmine Tartraterivastigmine tartrate
    0904-6587Rivastigmine TartrateRivastigmine Tartrate
    0904-7107Rivastigmine TartrateRivastigmine Tartrate
    27241-090RIVASTIGMINE TARTRATERIVASTIGMINE TARTRATE
    27241-091RIVASTIGMINE TARTRATERIVASTIGMINE TARTRATE
    27241-092RIVASTIGMINE TARTRATERIVASTIGMINE TARTRATE
    27241-093RIVASTIGMINE TARTRATERIVASTIGMINE TARTRATE
    33342-089RIVASTIGMINE TARTRATERIVASTIGMINE TARTRATE

    Trademark Results [Exelon]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    EXELON
    EXELON
    97977525 not registered Live/Pending
    Exelon Corporation
    2021-11-05
    EXELON
    EXELON
    97977523 not registered Live/Pending
    Exelon Corporation
    2021-11-05
    EXELON
    EXELON
    97110038 not registered Live/Pending
    Exelon Corporation
    2021-11-05
    EXELON
    EXELON
    97110036 not registered Live/Pending
    Exelon Corporation
    2021-11-05
    EXELON
    EXELON
    86776336 5508909 Live/Registered
    Exelon Corporation
    2015-10-02
    EXELON
    EXELON
    86776333 5508908 Live/Registered
    Exelon Corporation
    2015-10-02
    EXELON
    EXELON
    86302338 4671120 Live/Registered
    Exelon Corporation
    2014-06-06
    EXELON
    EXELON
    85982666 not registered Dead/Abandoned
    Exelon Corporation
    2012-05-24
    EXELON
    EXELON
    85982665 not registered Dead/Abandoned
    Exelon Corporation
    2012-05-24
    EXELON
    EXELON
    85980324 4445212 Live/Registered
    Exelon Corporation
    2012-05-24
    EXELON
    EXELON
    85980323 4445211 Live/Registered
    Exelon Corporation
    2012-05-24
    EXELON
    EXELON
    85634507 not registered Dead/Abandoned
    Exelon Corporation
    2012-05-24
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.