NDC 66651-101-13 - Thiabendazole

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
66651-101
Requested NDC
66651-101-13
Package NDCs from labels
66651-101-17, 66651-101-16, 66651-101-15, 66651-101-14, 66651-101-13, 66651-101-12, 66651-101-11
Manufacturer
HIKAL LIMITED
Effective date
2022-12-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Thiabendazole - HIKAL LIMITEDHIKAL LIMITED2022-12-11BULK INGREDIENT - ANIMAL DRUG

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

Reported adverse events (FAERS/openFDA)#

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