FDA.reportPublic FDA data

NDC 73377-091-01 - 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
73377-091
Requested NDC
73377-091-01
Package NDCs from labels
73377-091-01
Manufacturer
AX Pharmaceutical Corp
Effective date
2020-12-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Chloramphenicol Palmitate - AX Pharmaceutical CorpAX Pharmaceutical Corp2020-12-03BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-091-01Chloramphenicol Palmitate25 kg in 1 DRUMPOWDER251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-091CHLORAMPHENICOL PALMITATE POWDER [AX PHARMACEUTICAL CORP]11 package rows20201204_19d99747-4b6c-4db5-8877-59f4eb3a44b0.zip

Reported adverse events (FAERS/openFDA)#

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