NDC 0093-3060

Rasagiline

Rasagiline

Rasagiline is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Rasagiline Mesylate.

Product ID0093-3060_0c7edeb7-f1a4-4fa0-afed-6e037f785ed4
NDC0093-3060
Product TypeHuman Prescription Drug
Proprietary NameRasagiline
Generic NameRasagiline
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-01-03
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA021641
Labeler NameTeva Pharmaceuticals USA, Inc.
Substance NameRASAGILINE MESYLATE
Active Ingredient Strength1 mg/1
Pharm ClassesMonoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0093-3060-56

30 TABLET in 1 BOTTLE (0093-3060-56)
Marketing Start Date2017-01-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0093-3060-56 [00093306056]

Rasagiline TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA021641
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-01-03

Drug Details

Active Ingredients

IngredientStrength
RASAGILINE MESYLATE.5 mg/1

OpenFDA Data

SPL SET ID:e802c83c-e581-4a11-b83d-1df47120078d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 608328
  • 636664
  • Pharmacological Class

    • Monoamine Oxidase Inhibitor [EPC]
    • Monoamine Oxidase Inhibitors [MoA]

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

    NDCBrand NameGeneric Name
    0093-3060RasagilineRasagiline
    0093-3061RasagilineRasagiline
    16714-770RasagilineRasagiline
    16714-771RasagilineRasagiline
    42291-779RasagilineRasagiline
    42291-780RasagilineRasagiline
    42571-220RASAGILINERasagiline
    42571-221RASAGILINERasagiline
    47781-683RasagilineRasagiline
    47781-690RasagilineRasagiline
    67877-259RasagilineRasagiline
    67877-260RasagilineRasagiline

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