NDC 67850-011

Levetiracetam

Levetiracetam

Levetiracetam is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Methapharm, Inc.. The primary component is Levetiracetam.

Product ID67850-011_3c219760-e94e-de53-2b3a-2155fe2224b1
NDC67850-011
Product TypeHuman Prescription Drug
Proprietary NameLevetiracetam
Generic NameLevetiracetam
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-10-18
Marketing CategoryANDA / ANDA
Application NumberANDA090767
Labeler NameMethapharm, Inc.
Substance NameLEVETIRACETAM
Active Ingredient Strength250 mg/1
Pharm ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 67850-011-01

120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67850-011-01)
Marketing Start Date2010-10-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67850-011-01 [67850001101]

Levetiracetam TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090767
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-18
Marketing End Date2011-03-31
Inactivation Date2019-10-21
Reactivation Date2019-12-24

Drug Details

Active Ingredients

IngredientStrength
LEVETIRACETAM250 mg/1

OpenFDA Data

SPL SET ID:db0a1e4b-90b1-4754-9a6d-17042e54ce05
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311290
  • 387003
  • 311289
  • 311288
  • Pharmacological Class

    • Decreased Central Nervous System Disorganized Electrical Activity [PE]

    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.