RecallHawk

SEVELAMER CARBONATE

AUROBINDO PHARMA

Summary

FDA approved SEVELAMER CARBONATE by AUROBINDO PHARMA. ANDA (Generic) approval (Labeling) on 2024-04-30. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA207179-11

Action Date

2024-04-30

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

SEVELAMER CARBONATE, TABLET, ORAL. Application: ANDA207179

Context & Analysis

AUROBINDO PHARMA has 76 FDA actions in our database.

Frequently Asked Questions

How often does AUROBINDO PHARMA have FDA actions?

AUROBINDO PHARMA has 76 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 "ANDA207179-11" 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