RecallHawk

OCTREOSCAN (INDIUM IN -111 PENTETREOTIDE)

CURIUM

Summary

FDA approved OCTREOSCAN (INDIUM IN -111 PENTETREOTIDE) by CURIUM. NDA (New Drug) approval (Labeling) on 2022-02-09. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

NDA020314-12

Action Date

2022-02-09

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

OCTREOSCAN (generic: INDIUM IN -111 PENTETREOTIDE), INJECTABLE, INJECTION. Application: NDA020314

Company

Context & Analysis

CURIUM has 5 FDA actions in our database.

Frequently Asked Questions

How often does CURIUM have FDA actions?

CURIUM has 5 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA020314-12" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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