RecallHawk

SODIUM ACETATE ANHYDROUS

SOMERSET THERAPS LLC

Summary

FDA approved SODIUM ACETATE ANHYDROUS by SOMERSET THERAPS LLC. ANDA (Generic) approval on 2025-09-18. SOLUTION, INTRAVENOUS.

Details

Source

Drug Approval

External ID

ANDA219826-1

Action Date

2025-09-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

SODIUM ACETATE ANHYDROUS, SOLUTION, INTRAVENOUS. Application: ANDA219826

Context & Analysis

SOMERSET THERAPS LLC has 26 FDA actions in our database.

Frequently Asked Questions

How often does SOMERSET THERAPS LLC have FDA actions?

SOMERSET THERAPS LLC has 26 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 "ANDA219826-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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