NDC 10797-720 - BetaVet

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
10797-720
Package NDCs from labels
10797-720-01
Manufacturer
American Regent, Inc.
Effective date
2024-10-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
BetaVet - American Regent, Inc.American Regent, Inc.2024-10-07PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10797-720-01BetaVet1 in 1 CARTONINJECTION, SUSPENSION112
10797-720-01BetaVet5 mL in 1 VIALINJECTION, SUSPENSION512

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10797-720BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [AMERICAN REGENT, INC.]112 package rows20241009_3eb6b1d3-4485-4b25-aaab-92de9b2fb322.zip

DailyMed Socrata Ingredients#