RecallHawk

AMOXICILLIN

AUROBINDO

Summary

FDA approved AMOXICILLIN by AUROBINDO. ANDA (Generic) approval (Manufacturing (CMC)) on 2024-09-18. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA065256-27

Action Date

2024-09-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

AMOXICILLIN, TABLET, ORAL. Application: ANDA065256

Company

Context & Analysis

AUROBINDO has 4 FDA actions in our database.

Frequently Asked Questions

How often does AUROBINDO have FDA actions?

AUROBINDO has 4 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 "ANDA065256-27" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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