RecallHawk

IBUPROFEN AND FAMOTIDINE

ZYDUS LIFESCIENCES

Summary

FDA approved IBUPROFEN AND FAMOTIDINE by ZYDUS LIFESCIENCES. ANDA (Generic) approval on 2025-02-20. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA218684-1

Action Date

2025-02-20

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

IBUPROFEN AND FAMOTIDINE, TABLET, ORAL. Application: ANDA218684

Context & Analysis

ZYDUS LIFESCIENCES has 37 FDA actions in our database.

Frequently Asked Questions

How often does ZYDUS LIFESCIENCES have FDA actions?

ZYDUS LIFESCIENCES has 37 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 "ANDA218684-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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