NDC 0061-5354 - Sentinel Spectrum

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: 0061-5354
Package NDCs from labels: 0061-5354-01, 0061-5354-02
Manufacturer: Merck Sharp & Dohme Corp. | Virbac Corporation
Effective date: 2025-09-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sentinel Spectrum - Merck Sharp & Dohme Corp. \| Virbac Corporation	Merck Sharp & Dohme Corp. \| Virbac Corporation	2025-09-25	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0061-5354-01	Sentinel Spectrum	6 in 1 BLISTER PACK	TABLET, CHEWABLE	6	6
0061-5354-01	Sentinel Spectrum	1 in 1 CARTON	TABLET, CHEWABLE	1	6
0061-5354-02	Sentinel Spectrum	2 in 1 CARTON	TABLET, CHEWABLE	2	6
0061-5354-02	Sentinel Spectrum	6 in 1 BLISTER PACK	TABLET, CHEWABLE	6	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0061-5354	SENTINEL SPECTRUM (MILBEMYCIN OXIME, LUFENURON AND PRAZIQUANTEL) TABLET, CHEWABLE [MERCK SHARP & DOHME CORP.]	5	4 package rows	20241116_197a022a-bb94-4058-a4b7-96323e4b311e.zip

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.