FDA.reportPublic FDA data

NDC 58005-742 - Florfenicol

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
58005-742
Package NDCs from labels
58005-742-04, 58005-742-05, 58005-742-06
Manufacturer
Sparhawk Laboratories, Inc | Zhejiang Hisoar Pharmaceutical Co. Ltd.
Effective date
2023-11-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FLORFENICOL Injectable Solution 300 mg/mLSparhawk Laboratories, Inc | Zhejiang Hisoar Pharmaceutical Co. Ltd.2023-11-30PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58005-742-04Florfenicol100 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION1003
58005-742-05Florfenicol250 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION2503
58005-742-06Florfenicol500 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58005-742FLORFENICOL INJECTION, SOLUTION [SPARHAWK LABORATORIES, INC]33 package rows20231201_6fac13e9-69dd-464c-acbe-e20457b8b540.zip

Reported adverse events (FAERS/openFDA)#

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