FDA.reportPublic FDA data

NDC 73361-001 - Chloramphenicol Palmitate

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
73361-001
Package NDCs from labels
73361-001-01, 73361-001-02
Manufacturer
Wang Pharmaceuticals & Chemicals
Effective date
2020-07-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Chloramphenicol Palmitate - Wang Pharmaceuticals & ChemicalsWang Pharmaceuticals & Chemicals2020-07-06BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73361-001-01Chloramphenicol Palmitate25 kg in 1 DRUMPOWDER252
73361-001-02Chloramphenicol Palmitate5 kg in 1 BAGPOWDER52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73361-001CHLORAMPHENICOL PALMITATE POWDER [WANG PHARMACEUTICALS & CHEMICALS]22 package rows20200707_90f288c5-1c41-4d56-add4-50d458fa3e63.zip

Reported adverse events (FAERS/openFDA)#

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