RecallHawk

DILTIAZEM HYDROCHLORIDE

AMTA

Summary

FDA approved DILTIAZEM HYDROCHLORIDE by AMTA. ANDA (Generic) approval (Labeling) on 2026-01-18. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA216439-5

Action Date

2026-01-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DILTIAZEM HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA216439

Company

Context & Analysis

AMTA has 2 FDA actions in our database.

Frequently Asked Questions

How often does AMTA have FDA actions?

AMTA has 2 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 "ANDA216439-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions