NDC 0591-3635

Levetiracetam

Levetiracetam

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

Product ID0591-3635_392da1d3-de2e-46f0-b88b-1859c40dbb62
NDC0591-3635
Product TypeHuman Prescription Drug
Proprietary NameLevetiracetam
Generic NameLevetiracetam
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2011-09-12
Marketing End Date2019-03-31
Marketing CategoryANDA /
Application NumberANDA091093
Labeler NameActavis Pharma, Inc.
Substance NameLEVETIRACETAM
Active Ingredient Strength500 mg/1
Pharm ClassesDecreased Centr
NDC Exclude FlagN

Packaging

NDC SPL Data Element Entries

NDC 0591-3635-10 [00591363510]

Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA091093
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-09-12
Marketing End Date2011-09-12

NDC 0591-3635-05 [00591363505]

Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA091093
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-09-12
Marketing End Date2011-09-12

NDC 0591-3635-60 [00591363560]

Levetiracetam TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA091093
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-09-12
Marketing End Date2019-03-31

Drug Details

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.