RecallHawk

Summary

FDA approved OLANZAPINE by CADILA PHARMS LTD. ANDA (Generic) approval (Labeling) on 2026-01-22. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA210022-2

Action Date

2026-01-22

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

OLANZAPINE, TABLET, ORAL. Application: ANDA210022

Context & Analysis

CADILA PHARMS LTD has 9 FDA actions in our database.

Frequently Asked Questions

How often does CADILA PHARMS LTD have FDA actions?

CADILA PHARMS LTD has 9 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 "ANDA210022-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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