FDA.reportPublic FDA data

NDC 62991-3196-1 - OXANTEL PAMOATE

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
62991-3196
Requested NDC
62991-3196-1
Package NDCs from labels
62991-3196-1
Manufacturer
LETCO MEDICAL, LLC
Effective date
2024-07-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
OXANTEL PAMOATE - LETCO MEDICAL, LLCLETCO MEDICAL, LLC2024-07-18BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62991-3196-1OXANTEL PAMOATE20000 g in 1 DRUMPOWDER200003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62991-3196OXANTEL PAMOATE POWDER [LETCO MEDICAL, LLC]21 package rows20240719_a303d3b6-5083-4acd-ab43-4addeb1e270f.zip

Reported adverse events (FAERS/openFDA)#

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