RecallHawk

MAGNESIUM SULFATE (MAGNESIUM SULFATE IN WATER FOR)

AMNEAL

Summary

FDA approved MAGNESIUM SULFATE (MAGNESIUM SULFATE IN WATER FOR) by AMNEAL. ANDA (Generic) approval (Labeling) on 2023-07-12. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA216597-1

Action Date

2023-07-12

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MAGNESIUM SULFATE (generic: MAGNESIUM SULFATE IN WATER FOR), INJECTABLE, INJECTION. Application: ANDA216597

Company

Context & Analysis

AMNEAL has 70 FDA actions in our database.

Frequently Asked Questions

How often does AMNEAL have FDA actions?

AMNEAL 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 "ANDA216597-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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