NDC 51672-4136-07 - Levetiracetam

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51672-4136
Requested NDC
51672-4136-07
Package NDCs from labels
51672-4136-7, 51672-4136-9, 51672-4136-0, 51672-4136-07
Manufacturer
Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
Effective date
2026-03-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
LevetiracetamSun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.2026-03-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-4136-0Levetiracetam3785 mL in 1 BOTTLESOLUTION378515
51672-4136-7Levetiracetam100 mL in 1 BOTTLESOLUTION10015
51672-4136-9Levetiracetam473 mL in 1 BOTTLESOLUTION47315

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-4136LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]12Current NDC, Legacy NDC, 3 package rows20200723_bf412e94-ca36-4da9-83d7-fb0f1323cf21.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-4136-9ML - Milliliter51672-4136e160738e-4508-4a32-b72e-4b74171d8acd12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LevetiracetamACTIVE INGREDIENT44YRR34555LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
LevetiracetamACTIVE MOIETY44YRR34555LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
acesulfame potassiumINACTIVE INGREDIENT23OV73Q5G9LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
aluminum oxideINACTIVE INGREDIENTLMI26O6933LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
ammonium glycyrrhizateINACTIVE INGREDIENT3VRD35U26CLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
citric acid monohydrateINACTIVE INGREDIENT2968PHW8QPLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
FD&C Blue no. 2INACTIVE INGREDIENTL06K8R7DQKLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
ferric oxide redINACTIVE INGREDIENT1K09F3G675LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
ferric oxide yellowINACTIVE INGREDIENTEX438O2MRTLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
ferrosoferric oxideINACTIVE INGREDIENTXM0M87F357LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
glycerinINACTIVE INGREDIENTPDC6A3C0OXLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
hypromellosesINACTIVE INGREDIENT3NXW29V3WOLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
indigotindisulfonate sodiumINACTIVE INGREDIENTD3741U8K7LLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
magnesium stearateINACTIVE INGREDIENT70097M6I30LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
methylparabenINACTIVE INGREDIENTA2I8C7HI9TLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
polyethylene glycolsINACTIVE INGREDIENT3WJQ0SDW1ALEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
povidonesINACTIVE INGREDIENTFZ989GH94ELEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
propylparabenINACTIVE INGREDIENTZ8IX2SC1OHLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4LEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
starch, cornINACTIVE INGREDIENTO8232NY3SJLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
talcINACTIVE INGREDIENT7SEV7J4R1ULEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
trisodium citrate dihydrateINACTIVE INGREDIENTB22547B95KLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9
waterINACTIVE INGREDIENT059QF0KO0RLEVETIRACETAM TABLET, FILM COATED LEVETIRACETAM SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.]9

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 86 of 171 · 3,418 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
iVIZIA Dry EyePOVIDONEThea Pharma Inc.1ef73cb1-da48-a713-e063-6294a90afa9d2025-10-20WarningsExact identifier
unii: FZ989GH94E
Clinical Skin Filter Tinted SunscreenCLINICAL SKIN FILTER TINTED SUNSCREENKRX RESOURCES SDN. BHD.22b8856b-671f-def3-e063-6394a90a4ea02025-10-18WarningsExact identifier
unii: 15FIX9V2JP
Clinical Skin Filter Tinted Sunscreen Medium DarkCLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARKKRX RESOURCES SDN. BHD.22cead37-f862-e859-e063-6394a90a86ce2025-10-18WarningsExact identifier
unii: 15FIX9V2JP
Krx Aesthetics All Day Glow SunblockerKRX AESTHETICS ALL DAY GLOW SUNBLOCKERKRX RESOURCES SDN. BHD.22a60fb9-0fea-92c0-e063-6394a90a088c2025-10-18WarningsExact identifier
unii: 15FIX9V2JP
GlycerinGLYCERINChain Drug Consortium LLC4694f05b-d927-4e15-9630-a0a1cddb3cbb2025-10-16WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINAmerisource Bergen/Good Neighbor Pharmacye6a8914f-cfd9-4c72-abaa-22189bf0faef2025-10-16WarningsExact identifier
unii: PDC6A3C0OX
GlycerinGLYCERINChain Drug Marketing Association Inc.3386fada-6b7f-46fd-e063-6294a90abffc2025-10-16WarningsExact identifier
unii: PDC6A3C0OX
DD CreamDD CREAMDERMAdoctor, Inc.08c9a0cf-ee78-483b-e054-00144ff88e882025-10-16WarningsExact identifier
unii: 15FIX9V2JP
LevetiracetamLEVETIRACETAMA-S Medication Solutions671a1ae1-f672-48da-8a69-94c1474720032025-10-16Warnings, Adverse reactionsExact identifier
rxcui: 311289
unii: 44YRR34555
Ciele Filter and ProtectTITANIUM DIOXIDE, ZINC OXIDECiele0309b0ef-baca-b41d-e063-6294a90a49d72025-10-15WarningsExact identifier
unii: 15FIX9V2JP
Defend and Balance TInted Mineral Sunscreen SPF 50SUNSCREENEpicuren Discovery41367f05-59d8-6736-e063-6394a90a5f172025-10-15WarningsExact identifier
unii: 15FIX9V2JP
DENTI BUONGIORNO PEACH MINT WHITENING TOOTHHYDROGEN PEROXIDE, SILICAATOSAFE CO., Ltd41196c2f-8e2e-a54d-e063-6294a90ad8a72025-10-14WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO PEACH MINT WHITENING TOOTHHYDROGEN PEROXIDE, SILICADONG IL PHARMS CO.,LTD41198822-7c8f-ceb2-e063-6394a90a43732025-10-14WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO ORIGINAL TOOTHSILICA, SODIUM MONOFLUOROPHOSPHATEDONG IL PHARMS CO.,LTD41197bb6-f6f4-c86d-e063-6294a90ad4762025-10-14WarningsExact identifier
unii: ETJ7Z6XBU4
FinaftaBENZOCAINE, GLYCERINEfficient Laboratories Inc.03368603-3e11-c2fa-e063-6294a90a04ea2025-10-14WarningsExact identifier
unii: PDC6A3C0OX
Skinlycious Multi Protection Mineral Sunscreen Broad Spectrum SPF 30TITANIUM DIOXIDE , ZINC OXIDESkinlycious Pte Ltde0ad02c3-f5ed-4b72-ba96-07d9c489a4ea2025-10-13WarningsExact identifier
unii: 15FIX9V2JP
DENTI BUONGIORNO ORIGINAL TOOTHSILICA, SODIUM MONOFLUOROPHOSPHATEATOSAFE CO., Ltd4114ab09-1115-6b0b-e063-6394a90ab4422025-10-13WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATEATOSAFE CO., Ltd41155922-d7ac-0a7a-e063-6294a90afe482025-10-13WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATEDONG IL PHARMS CO.,LTD41157552-2473-176b-e063-6294a90a9ad02025-10-13WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATEATOSAFE CO., Ltd4115d122-3090-d3e5-e063-6294a90aafb62025-10-13WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.