NDC 54771-6870 - Synovex Primer

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: 54771-6870
Package NDCs from labels: 54771-6870-1
Manufacturer: Zoetis Inc.
Effective date: 2025-02-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SYNOVEX Primer ®	Zoetis Inc.	2025-02-21	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54771-6870-1	Synovex Primer	1 in 1 BOX	IMPLANT	1		2
54771-6870-1	Synovex Primer	10 in 1 POUCH	IMPLANT	10		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54771-6870	SYNOVEX PRIMER (TRENBOLONE ACETATE AND ESTRADIOL BENZOATE) IMPLANT [ZOETIS INC.]	2	2 package rows	20250223_8893799d-d617-43dc-bcd2-5604deadb694.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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Solvent/Small Ring Combination 9317	SOLVENT/SMALL RING COMBINATION	Professional Complementary Health Formulas	01a1b313-3edb-4907-9d9b-bb1d1061b4ef	2026-01-08	Warnings	Exact identifier unii: 1S4CJB5ZGN

Reported adverse events (FAERS/openFDA)#

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