NDC 43457-643 - PraziMed

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
43457-643
Package NDCs from labels
43457-643-10, 43457-643-11, 43457-643-50, 43457-643-51, 43457-643-25, 43457-643-26
Manufacturer
KDG Impresa LLC, Aqion
Effective date
2026-04-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PraziMed - KDG Impresa LLC, AqionKDG Impresa LLC, Aqion2026-04-03OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43457-643-10PraziMed10 g in 1 POUCHPOWDER104
43457-643-11PraziMed1 in 1 BOXPOWDER14
43457-643-25PraziMed250 g in 1 POUCHPOWDER2504
43457-643-26PraziMed1 in 1 JARPOWDER14
43457-643-50PraziMed50 g in 1 POUCHPOWDER504
43457-643-51PraziMed1 in 1 JARPOWDER14

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 1 of 1 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PRAZIQUANTELPRAZIQUANTELPar Health USA, LLC16f2b9c4-a260-4a31-bd52-e5945913246c2026-08-12Warnings, Adverse reactionsExact identifier
unii: 6490C9U457
BiltricidePRAZIQUANTELBayer HealthCare Pharmaceuticals Inc.34ce1cdd-648e-4f1e-8512-bf3d4cc22eb92026-03-02Warnings, Adverse reactionsExact identifier
unii: 6490C9U457

Reported adverse events (FAERS/openFDA)#

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