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COMBOGESIC IV (ACETAMINOPHEN AND IBUPROFEN INJECTION)

HIKMA

Summary

FDA approved COMBOGESIC IV (ACETAMINOPHEN AND IBUPROFEN INJECTION) by HIKMA. NDA (New Drug) approval (Labeling) on 2024-11-21. SOLUTION, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA215320-1

Action Date

2024-11-21

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

COMBOGESIC IV (generic: ACETAMINOPHEN AND IBUPROFEN INJECTION), SOLUTION, INTRAVENOUS. Application: NDA215320

Company

Context & Analysis

HIKMA has 117 FDA actions in our database.

Frequently Asked Questions

How often does HIKMA have FDA actions?

HIKMA has 117 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 "NDA215320-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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