NDC 69043-057 - DetomiSed

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
69043-057
Package NDCs from labels
69043-057-02
Manufacturer
Cronus Pharma LLC
Effective date
2025-04-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DetomiSed - Cronus Pharma LLCCronus Pharma LLC2025-04-02PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69043-057-02DetomiSed1 in 1 CARTONINJECTION11
69043-057-02DetomiSed20 mL in 1 VIAL, GLASSINJECTION201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69043-057DETOMISED (DETOMIDINE HYDROCHLORIDE) INJECTION [CRONUS PHARMA LLC]12 package rows20250406_7f92609c-b1d5-4166-92a1-86163b5aa3db.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sulfamethoxazole and TrimethoprimSULFAMETHOXAZOLE AND TRIMETHOPRIMCronus Pharma LLC1b5de94f-973a-4b5a-91d7-45e05be786502025-04-02Warnings, Adverse reactionsName fallback
manufacturer name: Cronus Pharma LLC
CephalexinCEPHALEXINCronus Pharma LLCa4e861e2-5803-4c4a-a962-92f5755e1ab52025-01-10Warnings, Adverse reactionsName fallback
manufacturer name: Cronus Pharma LLC
CEFPODOXIME PROXETILCEFPODOXIME PROXETILCronus Pharma LLCbc9c338c-1fc7-4bc2-a357-a78e433cbe9d2024-01-04Warnings, Adverse reactionsName fallback
manufacturer name: Cronus Pharma LLC

Reported adverse events (FAERS/openFDA)#

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