NDC 61133-8251-4 - AmproMed FOR CALVES

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
61133-8251
Requested NDC
61133-8251-4
Package NDCs from labels
61133-8251-3, 61133-8251-4
Manufacturer
Bimeda Inc. | Bimeda, Inc.
Effective date
2022-07-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AmproMed FOR CALVES - Bimeda Inc. | Bimeda, Inc.Bimeda Inc. | Bimeda, Inc.2022-07-05OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61133-8251-3AmproMed FOR CALVES3785 mL in 1 JUGSOLUTION378514
61133-8251-4AmproMed FOR CALVES473 mL in 1 BOTTLESOLUTION47314

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61133-8251AMPROMED FOR CALVES (AMPROLIUM) SOLUTION [BIMEDA INC.]142 package rows20220706_65dfe2b4-982d-4ffe-acad-165a50de6d0b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMPROLIUMACTIVE INGREDIENT95CO6N199QAMPROMED FOR CALVES (AMPROLIUM) SOLUTION [BIMEDA INC., DIVISION OF CROSS VETPHARM GROUP]8
AMPROLIUM IONACTIVE MOIETYH2T307KMZRAMPROMED FOR CALVES (AMPROLIUM) SOLUTION [BIMEDA INC., DIVISION OF CROSS VETPHARM GROUP]8

Reported adverse events (FAERS/openFDA)#

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