RecallHawk

DILTIAZEM HYDROCHLORIDE

EUGIA PHARMA

Summary

FDA approved DILTIAZEM HYDROCHLORIDE by EUGIA PHARMA. ANDA (Generic) approval on 2023-03-29. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA216552-1

Action Date

2023-03-29

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DILTIAZEM HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA216552

Context & Analysis

EUGIA PHARMA has 44 FDA actions in our database.

Frequently Asked Questions

How often does EUGIA PHARMA have FDA actions?

EUGIA PHARMA has 44 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 "ANDA216552-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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