NDC 55529-030 - Flunixin-S

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
55529-030
Package NDCs from labels
55529-030-02, 55529-030-04
Manufacturer
Norbrook Laboratories Limited | ISP Chemicals LLC
Effective date
2022-03-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Flunixin-S - Norbrook Laboratories Limited | ISP Chemicals LLCNorbrook Laboratories Limited | ISP Chemicals LLC2022-03-14PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55529-030-02Flunixin-S1 in 1 CARTONINJECTION, SOLUTION14
55529-030-02Flunixin-S100 mL in 1 VIAL, GLASSINJECTION, SOLUTION1004
55529-030-04Flunixin-S250 mL in 1 VIAL, GLASSINJECTION, SOLUTION2504
55529-030-04Flunixin-S1 in 1 CARTONINJECTION, SOLUTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55529-030FLUNIXIN-S (FLUNIXIN MEGLUMINE) INJECTION, SOLUTION [NORBROOK LABORATORIES LIMITED]44 package rows20220407_32900cc3-d85e-470e-b215-62d63e6b77aa.zip

DailyMed Socrata Ingredients#