RecallHawk

FAMOTIDINE

EPIC PHARMA LLC

Summary

FDA approved FAMOTIDINE by EPIC PHARMA LLC. ANDA (Generic) approval on 2024-10-16. FOR SUSPENSION, ORAL.

Details

Source

Drug Approval

External ID

ANDA218344-1

Action Date

2024-10-16

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

FAMOTIDINE, FOR SUSPENSION, ORAL. Application: ANDA218344

Context & Analysis

EPIC PHARMA LLC has 27 FDA actions in our database.

Frequently Asked Questions

How often does EPIC PHARMA LLC have FDA actions?

EPIC PHARMA LLC has 27 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 "ANDA218344-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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