RecallHawk

HYDROCORTISONE SODIUM SUCCINATE

CIPLA

Summary

FDA approved HYDROCORTISONE SODIUM SUCCINATE by CIPLA. ANDA (Generic) approval on 2024-09-05. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA214050-1

Action Date

2024-09-05

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

HYDROCORTISONE SODIUM SUCCINATE, INJECTABLE, INJECTION. Application: ANDA214050

Company

Context & Analysis

CIPLA has 40 FDA actions in our database, including 7 recalls.

Frequently Asked Questions

How often does CIPLA have FDA actions?

CIPLA has 40 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA214050-1" 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