NDC 51311-002-10 - Tulissin 25

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: 51311-002
Requested NDC: 51311-002-10
Package NDCs from labels: 51311-002-10, 51311-002-25
Manufacturer: Virbac AH, Inc.
Effective date: 2022-01-12
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Tulissin 25® (tulathromycin injection) Injectable Solution	Virbac AH, Inc.	2022-01-12	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51311-002-10	Tulissin 25	100 in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	100		2
51311-002-25	Tulissin 25	250 in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	250		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51311-002	TULISSIN 25 (TULATHROMYCIN) INJECTION, SOLUTION [VIRBAC AH, INC.]	2	2 package rows	20220113_82f08410-b5de-4f1c-a059-48747a4328fe.zip

Reported adverse events (FAERS/openFDA)#

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