FDA.reportPublic FDA data

NDC 71052-117-01 - 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
71052-117
Requested NDC
71052-117-01
Package NDCs from labels
71052-117-01, 71052-117-05, 71052-117-25
Manufacturer
DARMERICA, LLC
Effective date
2024-12-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Chloramphenicol Palmitate - DARMERICA, LLCDARMERICA, LLC2024-12-19BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-117-01Chloramphenicol Palmitate1 kg in 1 PACKAGEPOWDER12
71052-117-05Chloramphenicol Palmitate5 kg in 1 PACKAGEPOWDER52
71052-117-25Chloramphenicol Palmitate25 kg in 1 PACKAGEPOWDER252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-117CHLORAMPHENICOL PALMITATE POWDER [DARMERICA, LLC]23 package rows20241222_b1a91140-bd4c-404a-a4d1-0a96d05177b0.zip

Reported adverse events (FAERS/openFDA)#

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