NDC 61133-3401 - Tetroxy 343

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
61133-3401
Package NDCs from labels
61133-3401-1, 61133-3401-2, 61133-3401-3, 61133-3401-4
Manufacturer
Bimeda, Inc.
Effective date
2024-03-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tetroxy 343 - Bimeda, Inc.Bimeda, Inc.2024-03-28PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61133-3401-1Tetroxy 343135.5 g in 1 POUCHPOWDER135.515
61133-3401-2Tetroxy 343272.2 g in 1 POUCHPOWDER272.215
61133-3401-3Tetroxy 3432260 g in 1 PAILPOWDER226015
61133-3401-4Tetroxy 343907.2 g in 1 PAILPOWDER907.215

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61133-3401TETROXY 343 (OXYTETRACYCLINE HCL) POWDER [BIMEDA, INC.]154 package rows20240330_c1857237-3067-46f7-ab2a-710775a1a86d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
OXYTETRACYCLINE HYDROCHLORIDEACTIVE INGREDIENT4U7K4N52ZMTETROXY 343 (OXYTETRACYCLINE HCL) POWDER [BIMEDA, INC. DIVISION OF CROSS VETPHARM GROUP]5
OXYTETRACYCLINE ANHYDROUSACTIVE MOIETYSLF0D9077STETROXY 343 (OXYTETRACYCLINE HCL) POWDER [BIMEDA, INC. DIVISION OF CROSS VETPHARM GROUP]5

Reported adverse events (FAERS/openFDA)#

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