FDA.reportPublic FDA data

NDC 11695-2801 - Propofol

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
11695-2801
Package NDCs from labels
11695-2801-1
Manufacturer
Butler Animal Health Supply, LLC dba Covetrus North America | Ivaoes, LLC | CORDEN PHARMA SPA | Si Group, Inc.
Effective date
2023-12-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Propofol Injectable EmulsionButler Animal Health Supply, LLC dba Covetrus North America | Ivaoes, LLC | CORDEN PHARMA SPA | Si Group, Inc.2023-12-13PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11695-2801-1Propofol20 mL in 1 VIALINJECTION, EMULSION203
11695-2801-1Propofol5 in 1 CARTONINJECTION, EMULSION53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11695-2801PROPOFOL INJECTION, EMULSION [BUTLER ANIMAL HEALTH SUPPLY, LLC DBA COVETRUS NORTH AMERICA]32 package rows20231214_1fa84201-a1de-4780-b846-e2bef8b49be2.zip