RecallHawk

SPIRONOLACTONE

ANNORA PHARMA

Summary

FDA approved SPIRONOLACTONE by ANNORA PHARMA. ANDA (Generic) approval (Labeling) on 2026-05-12. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA217761-1

Action Date

2026-05-12

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

SPIRONOLACTONE, TABLET, ORAL. Application: ANDA217761

Context & Analysis

ANNORA PHARMA has 22 FDA actions in our database.

Frequently Asked Questions

How often does ANNORA PHARMA have FDA actions?

ANNORA PHARMA has 22 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 "ANDA217761-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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