RecallHawk

ATROPINE SULFATE

AM REGENT

Summary

FDA approved ATROPINE SULFATE by AM REGENT. ANDA (Generic) approval on 2022-05-26. SOLUTION, INTRAVENOUS.

Details

Source

Drug Approval

External ID

ANDA216120-1

Action Date

2022-05-26

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

ATROPINE SULFATE, SOLUTION, INTRAVENOUS. Application: ANDA216120

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 "ANDA216120-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions