NDC 0010-3309-02 - EQUIOXX

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: 0010-3309
Requested NDC: 0010-3309-02
Package NDCs from labels: 0010-3309-01, 0010-3309-02
Manufacturer: Boehringer Ingelheim Animal Health USA Inc.
Effective date: 2024-04-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Equioxx ® (firocoxib) Tablets 57 mg	Boehringer Ingelheim Animal Health USA Inc.	2024-04-01	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0010-3309-01	EQUIOXX	60 in 1 BOTTLE, PLASTIC	TABLET, CHEWABLE	60	2
0010-3309-01	EQUIOXX	1 in 1 CARTON	TABLET, CHEWABLE	1	2
0010-3309-02	EQUIOXX	1 in 1 CARTON	TABLET, CHEWABLE	1	2
0010-3309-02	EQUIOXX	180 in 1 BOTTLE, PLASTIC	TABLET, CHEWABLE	180	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0010-3309	EQUIOXX (FIROCOXIB) TABLET, CHEWABLE [BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC.]	2	4 package rows	20240331_3f891a61-ce58-4cc1-97e2-a161907ea8eb.zip

Reported adverse events (FAERS/openFDA)#

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