RecallHawk

NOREPINEPHRINE BITARTRATE

ANTHEA PHARMA

Summary

FDA approved NOREPINEPHRINE BITARTRATE by ANTHEA PHARMA. ANDA (Generic) approval on 2025-11-25. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA219924-1

Action Date

2025-11-25

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

NOREPINEPHRINE BITARTRATE, INJECTABLE, INJECTION. Application: ANDA219924

Context & Analysis

ANTHEA PHARMA has 2 FDA actions in our database.

Frequently Asked Questions

How often does ANTHEA PHARMA have FDA actions?

ANTHEA PHARMA has 2 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 "ANDA219924-1" 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