FDA.reportPublic FDA data

Thiabendazole

Manufacturer
HIKAL LIMITED
Effective date
2022-12-11
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
7
Source
full-release
Hydrated at
2026-06-01 02:50:36

Label at a glance#

ProductThiabendazole
Active ingredientThiabendazole
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Thiabendazole USP.jpgThiabendazole USP.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66651-101-11Thiabendazole1 kg in 1 DRUMPOWDER17
66651-101-12Thiabendazole2 kg in 1 DRUMPOWDER27
66651-101-13Thiabendazole5 kg in 1 DRUMPOWDER57
66651-101-14Thiabendazole10 kg in 1 DRUMPOWDER107
66651-101-15Thiabendazole25 kg in 1 DRUMPOWDER257
66651-101-16Thiabendazole30 kg in 1 DRUMPOWDER307
66651-101-17Thiabendazole50 kg in 1 DRUMPOWDER507

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66651-101THIABENDAZOLE POWDER [HIKAL LIMITED]77 package rows20221212_4e51db18-28ed-4038-ad60-166e1262304a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66651-10166651-101-17, 66651-101-16, 66651-101-15, 66651-101-14, 66651-101-13, 66651-101-12, 66651-101-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
ThiabendazoleN1Q45E87DTACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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