FDA.reportPublic FDA data

NDC 0641-6138-01 - Phenytoin Sodium

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
0641-6138
Requested NDC
0641-6138-01
Package NDCs from labels
0641-6138-01, 0641-6138-25
Manufacturer
Hikma Pharmaceuticals USA Inc.
Effective date
2024-04-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Phenytoin Sodium - Hikma Pharmaceuticals USA Inc.Hikma Pharmaceuticals USA Inc.2024-04-09HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-05-02Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0641-6138-01Phenytoin Sodium2 mL in 1 VIALINJECTION221
0641-6138-25Phenytoin Sodium25 in 1 CARTONINJECTION2521

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0641-6138PHENYTOIN SODIUM INJECTION [HIKMA PHARMACEUTICALS USA INC.]21Current NDC, Legacy NDC, 2 package rows20240410_8ad1be7b-a1a4-4a2a-bf9b-d22b350aa6e7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0641-6138-01ML - Milliliter0641-6138ec77a16e-2875-4829-86a7-607a0d096ec712013-05-02
0641-6138-25ML - Milliliter0641-6138a368c14d-8dab-409e-a72c-40f59da8cd7c12013-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHENYTOIN SODIUMACTIVE INGREDIENT4182431BJHPHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7
PHENYTOINACTIVE MOIETY6158TKW0C5PHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7
ALCOHOLINACTIVE INGREDIENT3K9958V90MPHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3PHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IPHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7
WATERINACTIVE INGREDIENT059QF0KO0RPHENYTOIN SODIUM INJECTION [WEST-WARD PHARMACEUTICAL CORP.]7

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 74 of 153 · 3,046 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WhiskCare 375ALCOHOLWhisk Products, Inc.63c61968-73d7-4d31-9604-e56748b990fa2025-11-11WarningsExact identifier
unii: 3K9958V90M
Walgreens Hand Sanitizer Sweet PeaALCOHOLShenzhen Lantern Scicence Co.,Ltd.435ca082-0b6b-c55e-e063-6294a90af56e2025-11-11WarningsExact identifier
unii: 3K9958V90M
Smart Care Hand Sanitizer BarbieALCOHOLShenzhen Lantern Scicence Co.,Ltd.435d514e-204a-118b-e063-6294a90aa8a62025-11-11WarningsExact identifier
unii: 3K9958V90M
Smart Care Hand Sanitizer Spider-manALCOHOLShenzhen Lantern Scicence Co.,Ltd.435d939c-9bef-bf86-e063-6394a90a41422025-11-11WarningsExact identifier
unii: 3K9958V90M
Smart Care SPIDER-MAN HAND SANITIZERETHYL ALCOHOLAshtel Studios, Inc.58cec7e5-65f9-4b39-a1a0-453fb293fe252025-11-11WarningsExact identifier
unii: 3K9958V90M
FOOTSPA PEDIALCOHOLCHEMCO CORPORATION04de4392-74f6-7df8-e063-6294a90ae3b12025-11-08WarningsExact identifier
unii: 3K9958V90M
Phenytoin SodiumPHENYTOIN SODIUMProPharma Distribution43060ca9-58a7-3371-e063-6294a90a57992025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA084307
rxcui: 1670351
unii: 4182431BJH
Surface x Cutie Pals Hand Sanitizer Cherry ColaALCOHOLLongway Technology(Guangzhou)Co., Ltd.635f1363-cd21-4d3c-8326-62c39fbd12ab2025-11-07WarningsExact identifier
unii: 3K9958V90M
Genuine First Aid Hand SanitizerALCOHOLGFA Production(Xiamen) Co.,Ltd0aaee809-d251-6119-e063-6294a90aee7a2025-11-07WarningsExact identifier
unii: 3K9958V90M
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Smart Care VANILLA VERDANT HAND SANITIZERETHYL ALCOHOLAshtel Studios Inc.ccf2f735-19ca-47b0-9343-0353a556dc112025-11-07WarningsExact identifier
unii: 3K9958V90M
PURELL Hand Sanitizing Wipes Alcohol FormulaALCOHOLGOJO Industries, Inc.390859de-2d8d-40f8-a0fc-05f7644e266c2025-11-06WarningsExact identifier
unii: 3K9958V90M
MedlineETHYL ALCOHOLMedline Industries, LP11fcc7e7-dfae-ee7d-e063-6294a90a3b312025-11-06WarningsExact identifier
unii: 3K9958V90M
Phenytoin SodiumPHENYTOIN SODIUMHenry Schein, Inc.889dd22c-46f0-48d0-b18e-a3783c5fa6532025-11-06Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA084307
rxcui: 1670351
unii: 4182431BJH
SMARTIES ORANGE HAND SANITIZER MIX BERRYALCOHOL ANTISEPTICKingkey MBC Life Technology Group Co.,Ltd42d5785f-a86b-47fb-e063-6294a90a73142025-11-05WarningsExact identifier
unii: 3K9958V90M
Sour Patch Kids Hand Sanitizer Blue RaspberryALCOHOL ANTISEPTICKingkey MBC Life Technology Group Co.,Ltd42d5afab-e872-09e3-e063-6394a90abcc42025-11-05WarningsExact identifier
unii: 3K9958V90M
DASIY HAND SANITIZERALCOHOL ANTISEPTICKingkey MBC Life Technology Group Co.,Ltd42d632d1-17a9-b4cf-e063-6394a90a84682025-11-05WarningsExact identifier
unii: 3K9958V90M
DASIY HAND SANITIZERALCOHOL ANTISEPTICKingkey MBC Life Technology Group Co.,Ltd42d677a4-3cc2-a039-e063-6294a90a16722025-11-05WarningsExact identifier
unii: 3K9958V90M
Bacteriostatic WaterBACTERIOSTATIC WATERProPharma Distribution42c6938e-f747-ae13-e063-6294a90a59a32025-11-04Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
San-EZ Hand SanitizerETHYL ALCOHOL 70%Dental Technologies, Inc.a2cca707-103d-7265-e053-2995a90aebfc2025-11-04WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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