NDC 68180-099

levetiracetam

Levetiracetam

levetiracetam is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is Levetiracetam.

Product ID68180-099_1b80dbd7-8ebc-49af-8160-3e65c46a6242
NDC68180-099
Product TypeHuman Prescription Drug
Proprietary Namelevetiracetam
Generic NameLevetiracetam
Dosage FormSolution
Route of AdministrationORAL
Marketing Start Date2014-11-01
Marketing CategoryANDA / ANDA
Application NumberANDA090893
Labeler NameLupin Pharmaceuticals, Inc.
Substance NameLEVETIRACETAM
Active Ingredient Strength100 mg/mL
Pharm ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68180-099-01

473 mL in 1 BOTTLE (68180-099-01)
Marketing Start Date2014-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68180-099-01 [68180009901]

levetiracetam SOLUTION
Marketing CategoryANDA
Application NumberANDA090893
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-11-01

Drug Details

Active Ingredients

IngredientStrength
LEVETIRACETAM100 mg/mL

OpenFDA Data

SPL SET ID:cdd6b1d1-e967-4a97-aea6-66126d1dffe1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 403884
  • UPC Code
  • 0368180099017
  • Pharmacological Class

    • Decreased Central Nervous System Disorganized Electrical Activity [PE]

    Medicade Reported Pricing

    68180009901 LEVETIRACETAM 100 MG/ML SOLN

    Pricing Unit: ML | Drug Type:

    NDC Crossover Matching brand name "levetiracetam" or generic name "Levetiracetam"

    NDCBrand NameGeneric Name
    0054-0224LevetiracetamLevetiracetam
    0121-0799LevetiracetamLEVETIRACETAM
    0121-1598LevetiracetamLEVETIRACETAM
    0121-2397LevetiracetamLEVETIRACETAM
    0121-4799LevetiracetamLEVETIRACETAM
    0121-4802LEVETIRACETAMLEVETIRACETAM
    0143-9574LevetiracetamLevetiracetam
    0143-9673LevetiracetamLevetiracetam
    0228-2167LevetiracetamLevetiracetam
    0378-5613Levetiracetamlevetiracetam
    0378-5615Levetiracetamlevetiracetam
    0378-5617Levetiracetamlevetiracetam
    67850-012LevetiracetamLevetiracetam
    67850-014LevetiracetamLevetiracetam
    67850-013LevetiracetamLevetiracetam
    67850-011LevetiracetamLevetiracetam
    68001-116LevetiracetamLevetiracetam
    68001-113LevetiracetamLevetiracetam
    68001-115LevetiracetamLevetiracetam
    68001-114LevetiracetamLevetiracetam
    68001-117LevetiracetamLevetiracetam
    68001-118LevetiracetamLevetiracetam
    68071-4508LevetiracetamLevetiracetam
    68083-153LevetiracetamLevetiracetam
    68083-154LevetiracetamLevetiracetam
    68083-152LevetiracetamLevetiracetam
    68084-870LevetiracetamLevetiracetam
    68084-859LevetiracetamLevetiracetam
    68084-893LevetiracetamLevetiracetam
    68084-882LevetiracetamLevetiracetam
    68180-118LevetiracetamLevetiracetam
    68180-113LevetiracetamLevetiracetam
    68180-115LevetiracetamLevetiracetam
    68180-117LevetiracetamLevetiracetam
    68180-112LevetiracetamLevetiracetam
    68180-114LevetiracetamLevetiracetam
    68180-099levetiracetamlevetiracetam
    68258-7089LevetiracetamLevetiracetam
    68382-165levetiracetamlevetiracetam
    68382-168levetiracetamlevetiracetam
    0472-0235LevetiracetamLevetiracetam
    68788-7074LevetiracetamLevetiracetam
    68788-6798LevetiracetamLevetiracetam
    68788-6838LevetiracetamLevetiracetam
    68788-7190LevetiracetamLevetiracetam
    68788-6966LevetiracetamLevetiracetam
    69076-750LevetiracetamLevetiracetam
    69076-500LevetiracetamLevetiracetam
    70518-0197LevetiracetamLevetiracetam
    70518-0365LevetiracetamLevetiracetam

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.