FDA.reportPublic FDA data

NDC 61133-8001 - SMZ-Med 454

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
61133-8001
Package NDCs from labels
61133-8001-1
Manufacturer
Bimeda, Inc. | Bimeda, Inc. Division of Cross Vetpharm Group Ltd.
Effective date
2024-04-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SMZ-Med 454 - Bimeda, Inc. | Bimeda, Inc. Division of Cross Vetpharm Group Ltd.Bimeda, Inc. | Bimeda, Inc. Division of Cross Vetpharm Group Ltd.2024-04-23PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61133-8001-1SMZ-Med 454453.5 g in 1 POUCHPOWDER453.515

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61133-8001SMZ-MED 454 (SODIUM SULFAMETHAZINE) POWDER [BIMEDA, INC.]151 package rows20240424_9ae5dab7-d2a5-4631-a51b-1aa93bba88fa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SulfamethazineACTIVE INGREDIENT48U51W007FSMZ-MED 454 (SODIUM SULFAMETHAZINE) POWDER [BIMEDA, INC. DIVISION OF CROSS VETPHARM GROUP LTD.]7
SULFAMETHAZINEACTIVE MOIETY48U51W007FSMZ-MED 454 (SODIUM SULFAMETHAZINE) POWDER [BIMEDA, INC. DIVISION OF CROSS VETPHARM GROUP LTD.]7

Reported adverse events (FAERS/openFDA)#

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