NDC 54771-1005-0 - Aureomycin

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
54771-1005
Requested NDC
54771-1005-0
Package NDCs from labels
54771-1005-0
Manufacturer
Zoetis Inc.
Effective date
2023-05-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Aureomycin ® 90 GranularZoetis Inc.2023-05-31VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54771-1005-0Aureomycin22.68 kg in 1 BAGGRANULE22.685

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54771-1005AUREOMYCIN (CHLORTETRACYCLINE HYDROCHLORIDE) GRANULE [ZOETIS INC.]51 package rows20230602_72ed9cb2-8eb6-4aee-a500-43abbc301d44.zip

Reported adverse events (FAERS/openFDA)#

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