RecallHawk

FENOFIBRATE (MICRONIZED)

PHARMOBEDIENT

Summary

FDA approved FENOFIBRATE (MICRONIZED) by PHARMOBEDIENT. ANDA (Generic) approval (Labeling) on 2022-01-04. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA202579-7

Action Date

2022-01-04

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

FENOFIBRATE (MICRONIZED), CAPSULE, ORAL. Application: ANDA202579

Context & Analysis

PHARMOBEDIENT has 49 FDA actions in our database.

Frequently Asked Questions

How often does PHARMOBEDIENT have FDA actions?

PHARMOBEDIENT has 49 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 "ANDA202579-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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