NDC 0859-2238 - Droncit

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: 0859-2238
Package NDCs from labels: 0859-2238-01, 0859-2238-03, 0859-2238-02, 0859-2238-04
Manufacturer: Bayer HealthCare LLC Animal Health Division
Effective date: 2020-12-02
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Droncit - Bayer HealthCare LLC Animal Health Division	Bayer HealthCare LLC Animal Health Division	2020-12-02	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
PRAZIQUANTEL	ACTIVE INGREDIENT	6490C9U457	DRONCIT (PRAZIQUANTEL) INJECTION, SOLUTION [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION]	4
PRAZIQUANTEL	ACTIVE MOIETY	6490C9U457	DRONCIT (PRAZIQUANTEL) INJECTION, SOLUTION [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION]	4

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PRAZIQUANTEL	PRAZIQUANTEL	Par Health USA, LLC	16f2b9c4-a260-4a31-bd52-e5945913246c	2026-08-12	Warnings, Adverse reactions	Exact identifier unii: 6490C9U457
Biltricide	PRAZIQUANTEL	Bayer HealthCare Pharmaceuticals Inc.	34ce1cdd-648e-4f1e-8512-bf3d4cc22eb9	2026-03-02	Warnings, Adverse reactions	Exact identifier unii: 6490C9U457

Reported adverse events (FAERS/openFDA)#

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