Home NDC 0641-2555-41 NDC 0641-2555-41 - 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 0641-2555
Requested NDC 0641-2555-41
Package NDCs from labels 0641-2555-41, 0641-2555-10, 0641-2555-45
Manufacturer Henry Schein, Inc.
Effective date 2024-12-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type PHENYTOIN SODIUM - Henry Schein, Inc. Henry Schein, Inc. 2024-12-26 HUMAN PRESCRIPTION DRUG LABEL Phenytoin Sodium - Henry Schein, Inc. Henry Schein, Inc. 2024-08-19 HUMAN PRESCRIPTION DRUG LABEL Phenytoin Sodium - Hikma Pharmaceuticals USA Inc. Hikma Pharmaceuticals USA Inc. 2024-04-09 HUMAN PRESCRIPTION DRUG LABEL Phenytoin Sodium - General Injectables & Vaccines, Inc. General Injectables & Vaccines, Inc. 2022-12-29 HUMAN PRESCRIPTION DRUG LABEL PHENYTOIN SODIUM - HF Acquisition Co LLC, DBA HealthFirst HF Acquisition Co LLC, DBA HealthFirst 2022-12-09 HUMAN PRESCRIPTION DRUG LABEL National Council for Prescription Drug Programs indexing - billing unit National Council for Prescription Drug Programs 2012-07-24 Indexing - Billing Unit
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0641-2555-10 Phenytoin Sodium 10 in 1 CARTON INJECTION 10 27 0641-2555-41 Phenytoin Sodium 5 mL in 1 VIAL INJECTION 5 27 0641-2555-45 Phenytoin Sodium 25 in 1 CARTON INJECTION 25 27
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0641-2555 PHENYTOIN SODIUM INJECTION [HIKMA PHARMACEUTICALS USA INC.] 27 Current NDC, Legacy NDC, 3 package rows 20240410_035a8d4e-2063-4240-83cb-d7eebcabe301.zip
DailyMed Socrata Ingredients# 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 20 of 153 · 3,054 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Pink Peach Blossom ALCOHOL Bath & Body Works, Inc. 552feb22-c355-0572-e063-6394a90afa8c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunshine and Lemons ALCOHOL Bath & Body Works, Inc. 552fccdd-93c4-efff-e063-6294a90a54ba 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberry Tangerine ALCOHOL Bath & Body Works, Inc. 552fe6d9-335d-0842-e063-6394a90a9845 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Marine Waves and Citrus ALCOHOL Bath & Body Works, Inc. 552fe62e-5e18-1fed-e063-6294a90a489e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Watermelon Lemonade ALCOHOL Bath & Body Works, Inc. 552fe6d9-335f-0842-e063-6394a90a9845 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Turquoise Waters ALCOHOL Bath & Body Works, Inc. 552fe62e-5e1e-1fed-e063-6294a90a489e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Eucalyptus Rain ALCOHOL Bath & Body Works, Inc. 552ff8dc-b386-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Waikiki Beach Coconut ALCOHOL Bath & Body Works, Inc. 552fe62e-5e1d-1fed-e063-6294a90a489e 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Pineapple Sunrise ALCOHOL Bath & Body Works, Inc. 552fed13-f326-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Moisturizing Hand Sanitizer Coconut Pina Colada ALCOHOL Bath & Body Works, Inc. 552fe733-25f7-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 552fed13-f323-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Firecracker Pop ALCOHOL Bath & Body Works, Inc. 552ff8dc-b388-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Japanese Cherry Blossom ALCOHOL Bath & Body Works, Inc. 552fe733-25f9-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pineapple Mango ALCOHOL Bath & Body Works, Inc. 552fe733-25fc-30a7-e063-6294a90a4464 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Peach Blossom and Nectar ALCOHOL Bath & Body Works, Inc. 552feb22-c34c-0572-e063-6394a90afa8c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Butterfly ALCOHOL Bath & Body Works, Inc. 552ff81f-28d9-0f6e-e063-6394a90ab583 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Kiwi ALCOHOL Bath & Body Works, Inc. 552fe584-b74d-00ad-e063-6394a90a68e7 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Cut Lilacs ALCOHOL Bath & Body Works, Inc. 552feb22-c353-0572-e063-6394a90afa8c 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pink Kiwi Berry ALCOHOL Bath & Body Works, Inc. 552ff8dc-b387-0c47-e063-6394a90a47c3 2026-06-26 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Watermelon ALCOHOL Bath & Body Works, Inc. 552fed13-f329-27bc-e063-6294a90ae131 2026-06-26 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.