NDC 61133-6007 - Flunazine

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
61133-6007
Package NDCs from labels
61133-6007-1
Manufacturer
Bimeda Inc. | Bimeda-MTC Animal Health
Effective date
2024-03-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Flunazine - Bimeda Inc. | Bimeda-MTC Animal HealthBimeda Inc. | Bimeda-MTC Animal Health2024-03-13PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61133-6007-1Flunazine30 g in 1 SYRINGEPASTE309

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61133-6007FLUNAZINE (FLUNIXIN MEGLUMINE) PASTE [BIMEDA INC.]91 package rows20240315_ef38da06-9556-4841-8a72-e57c1f8a3e28.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FLUNIXIN MEGLUMINEACTIVE INGREDIENT8Y3JK0JW3UFLUNAZINE (FLUNIXIN MEGLUMINE) PASTE [BIMEDA INC DIVISION OF CROSVETPHARM]5
FLUNIXINACTIVE MOIETY356IB1O400FLUNAZINE (FLUNIXIN MEGLUMINE) PASTE [BIMEDA INC DIVISION OF CROSVETPHARM]5

Reported adverse events (FAERS/openFDA)#

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