NDC 86121-0003 - Laverdia-CA1

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
86121-0003
Package NDCs from labels
86121-0003-1, 86121-0003-2
Manufacturer
Anivive Lifesciences, Inc
Effective date
2022-02-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Laverdia-CA1 - Anivive Lifesciences, IncAnivive Lifesciences, Inc2022-02-22PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86121-0003-1Laverdia-CA150 in 1 BOTTLE, PLASTICTABLET, COATED504
86121-0003-1Laverdia-CA11 in 1 CARTONTABLET, COATED14
86121-0003-2Laverdia-CA116 in 1 BOTTLE, PLASTICTABLET, COATED164
86121-0003-2Laverdia-CA11 in 1 CARTONTABLET, COATED14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86121-0003LAVERDIA-CA1 (VERDINEXOR) TABLET, COATED [ANIVIVE LIFESCIENCES, INC]44 package rows20220310_b4e1ffc1-3518-4061-8ee1-5195b0302965.zip