Levetiracetam

Product NDC
71335-2275
11-digit product format
713352275
Labeler code
71335
Product ID
71335-2275_713cf359-1aa0-47df-94cb-fbf6d4a7aa9a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Levetiracetam
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091491
Marketing category
ANDA
Marketing start
2023-05-01
Substance
LEVETIRACETAM
Active strength
250 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
44YRR34555LEVETIRACETAM102767-28-2LEVETIRACETAM

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2275-17133522750160 TABLET in 1 BOTTLE (71335-2275-1) 60 tablet2024-05-30NoNoHistorical
71335-2275-27133522750230 TABLET in 1 BOTTLE (71335-2275-2) 30 tablet2023-12-28NoNoHistorical
71335-2275-371335227503120 TABLET in 1 BOTTLE (71335-2275-3) 120 tablet2024-05-30NoNoHistorical
71335-2275-47133522750490 TABLET in 1 BOTTLE (71335-2275-4) 90 tablet2024-05-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LevetiracetamBryant Ranch Prepack2026-05-15HUMAN PRESCRIPTION DRUG LABEL102