RecallHawk

POTASSIUM PHOSPHATES

FRESENIUS KABI USA

Summary

FDA approved POTASSIUM PHOSPHATES by FRESENIUS KABI USA. NDA (New Drug) approval (Manufacturing (CMC)) on 2024-08-30. SOLUTION, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA212832-2

Action Date

2024-08-30

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

POTASSIUM PHOSPHATES, SOLUTION, INTRAVENOUS. Application: NDA212832

Context & Analysis

FRESENIUS KABI USA has 70 FDA actions in our database.

Frequently Asked Questions

How often does FRESENIUS KABI USA have FDA actions?

FRESENIUS KABI USA has 70 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 "NDA212832-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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