FDA.reportPublic FDA data

NDC 72969-110 - 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
72969-110
Package NDCs from labels
72969-110-10
Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2021-03-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FLORFENICOL - PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLCPROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC2021-03-29BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72969-110-10FLORFENICOL1 g in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72969-110FLORFENICOL POWDER [PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC]11 package rows20210401_a4b2bd25-cf1c-49e2-ab00-f969b06342a7.zip

Reported adverse events (FAERS/openFDA)#

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