NDC 59762-2350

Ethosuximide

Ethosuximide

Ethosuximide is a Oral Solution in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Ethosuximide.

Product ID59762-2350_2646752a-b2e8-4167-bf80-6ed8fa869917
NDC59762-2350
Product TypeHuman Prescription Drug
Proprietary NameEthosuximide
Generic NameEthosuximide
Dosage FormSolution
Route of AdministrationORAL
Marketing Start Date2020-02-21
Marketing CategoryANDA / ANDA
Application NumberANDA080258
Labeler NameGreenstone LLC
Substance NameETHOSUXIMIDE
Active Ingredient Strength250 mg/5mL
Pharm ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 59762-2350-6

1 BOTTLE, PLASTIC in 1 CARTON (59762-2350-6) > 474 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2020-02-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59762-2350-6 [59762235006]

Ethosuximide SOLUTION
Marketing CategoryANDA
Application NumberANDA080258
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2020-02-21

NDC 59762-2350-5 [59762235005]

Ethosuximide SOLUTION
Marketing CategoryANDA
Application NumberANDA080258
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2015-09-29
Marketing End Date2021-07-31

Drug Details

Active Ingredients

IngredientStrength
ETHOSUXIMIDE250 mg/5mL

OpenFDA Data

SPL SET ID:19c924c2-f558-4c78-9277-2d7e0df2f505
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 251322

    • Pharmacological Class

    • Anti-epileptic Agent [EPC]
    • Decreased Central Nervous System Disorganized Electrical Activity [PE]

    Medicade Reported Pricing

    59762235005 ETHOSUXIMIDE 250 MG/5 ML SOLN

    Pricing Unit: ML | Drug Type:

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

    NDCBrand NameGeneric Name
    0093-9660EthosuximideEthosuximide
    0121-0670ETHOSUXIMIDEETHOSUXIMIDE
    23155-532ETHOSUXIMIDEETHOSUXIMIDE
    42806-711EthosuximideEthosuximide
    46672-641ethosuximideethosuximide
    59762-2250EthosuximideEthosuximide
    59762-2350EthosuximideEthosuximide
    61748-024EthosuximideEthosuximide
    61748-025EthosuximideEthosuximide
    63629-8005EthosuximideEthosuximide
    64380-878ETHOSUXIMIDEETHOSUXIMIDE
    68382-443ethosuximideethosuximide
    69387-108EthosuximideEthosuximide
    69452-152EthosuximideEthosuximide
    71335-1763ETHOSUXIMIDEETHOSUXIMIDE
    0071-0237ZarontinEthosuximide
    0071-2418ZarontinEthosuximide
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.