FDA.reportPublic FDA data

NDC 45567-0753 - Kit for the Preparation of Indium In 111 Pentetreotide

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
45567-0753
Package NDCs from labels
45567-0753-1
Manufacturer
Sun Pharmaceutical Industries, Inc.
Effective date
2025-04-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Indium In-111 Pentetreotide - Sun Pharmaceutical Industries, Inc.Sun Pharmaceutical Industries, Inc.2025-04-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45567-0753-1Kit for the Preparation of Indium In 111 Pentetreotide1 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,1 mL10 ug in 1mL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45567-0753KIT FOR THE PREPARATION OF INDIUM IN 111 PENTETREOTIDE (INDIUM IN-111 PENTETREOTIDE) KIT [SUN PHARMACEUTICAL INDUSTRIES, INC.]12Unmatched20250424_e2117bbd-9db3-4d20-a5da-89551c18a0cb.zip