RecallHawk

EPINEPHRINE

AM REGENT

Summary

FDA approved EPINEPHRINE by AM REGENT. ANDA (Generic) approval (Labeling) on 2025-02-28. SOLUTION, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

ANDA207568-4

Action Date

2025-02-28

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

EPINEPHRINE, SOLUTION, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA207568

Company

Context & Analysis

AM REGENT has 14 FDA actions in our database.

Frequently Asked Questions

How often does AM REGENT have FDA actions?

AM REGENT has 14 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 "ANDA207568-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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