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 44 of 153 · 3,045 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Mahogany Teakwood ALCOHOL Bath & Body Works, Inc. 1bba8dfa-947c-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Strawberry Pound Cake ALCOHOL Bath & Body Works, Inc. 1bba8dfa-947f-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel A Thousand Wishes ALCOHOL Bath & Body Works, Inc. 29a539bb-42e3-dc73-e063-6394a90a5fe9 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Peach Bellini ALCOHOL Bath & Body Works, Inc. 2b1124a3-9b14-07b6-e063-6394a90a4973 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Watermelon Lemonade ALCOHOL Bath & Body Works, Inc. 38e1bd3f-8e6e-7b68-e063-6394a90a8274 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sunshine and Lemons ALCOHOL Bath & Body Works, Inc. 1bba8dfa-9481-1ee2-e063-6294a90ae52a 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Midnight Blue Citrus ALCOHOL Bath & Body Works, Inc. 2b116b79-fe71-325a-e063-6394a90a045b 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Warm Vanilla Sugar ALCOHOL Bath & Body Works, Inc. 38d6f6a0-52bf-df77-e063-6394a90a4464 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Crystal Blue Coast ALCOHOL Bath & Body Works, Inc. 38e1480e-d217-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberry Tangerine ALCOHOL Bath & Body Works, Inc. 38e1cc04-7905-74e4-e063-6394a90a7b4c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Backyard Honeysuckle ALCOHOL Bath & Body Works, Inc. 38e1480e-d21c-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fresh Rainfall ALCOHOL Bath & Body Works, Inc. 38e1480e-d21d-7b66-e063-6394a90abfe5 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Raspberries and Whipped Vanilla ALCOHOL Bath & Body Works, Inc. 38e1cef4-4814-745c-e063-6394a90aebf0 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Fiji White Sands ALCOHOL Bath & Body Works, Inc. 38e1c1d6-6505-4066-e063-6294a90ad3f4 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweetest Song ALCOHOL Bath & Body Works, Inc. 38e1d907-75d7-3906-e063-6294a90a2ed7 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Endless Weekend ALCOHOL Bath & Body Works, Inc. 38e15918-9ee2-4061-e063-6294a90a881c 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Pina Colada Swirl ALCOHOL Bath & Body Works, Inc. 38e1e122-2087-90fa-e063-6394a90ab625 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Eucalyptus and Spearmint ALCOHOL Bath & Body Works, Inc. 38e1f8da-2003-80ba-e063-6394a90a2d1d 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Sweet Orange and Agave ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f10-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Book Loft ALCOHOL Bath & Body Works, Inc. 38e1d8fc-6f11-49d6-e063-6294a90a25ab 2026-03-09 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.