NDC 50604-7209 - 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
50604-7209
Package NDCs from labels
50604-7209-1
Manufacturer
Merial, Inc.
Effective date
2016-11-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Equioxx ® Injection (firocoxib)Merial, Inc.2016-11-21PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
firocoxibACTIVE INGREDIENTY6V2W4S4WTEQUIOXX (FIROCOXIB) INJECTION, SOLUTION [MERIAL LIMITED]4
firocoxibACTIVE MOIETYY6V2W4S4WTEQUIOXX (FIROCOXIB) INJECTION, SOLUTION [MERIAL LIMITED]4
glycerol formalINACTIVE INGREDIENT3L7GR2604EEQUIOXX (FIROCOXIB) INJECTION, SOLUTION [MERIAL LIMITED]4
Polyethylene Glycol 400INACTIVE INGREDIENTB697894SGQEQUIOXX (FIROCOXIB) INJECTION, SOLUTION [MERIAL LIMITED]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 7 of 7 · 122 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AnubisMedAZELAIC ACID, SALICYLIC ACIDANUBIS COSMETICS SLebf3153d-30f5-54e4-e053-2995a90a74b12023-09-05WarningsExact identifier
unii: B697894SGQ
Anubis Barcelona Protective LineETHYLHEXYL METHOXYCINNAMATE, BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, OCTOCRYLENEANUBIS COSMETICS SLec83846f-11c0-8f59-e053-2995a90ab9d22023-09-01WarningsExact identifier
unii: B697894SGQ

Reported adverse events (FAERS/openFDA)#

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