RecallHawk

DOXORUBICIN HYDROCHLORIDE

ALMAJECT

Summary

FDA approved DOXORUBICIN HYDROCHLORIDE by ALMAJECT. ANDA (Generic) approval (Labeling) on 2025-06-25. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA065515-3

Action Date

2025-06-25

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DOXORUBICIN HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA065515

Company

Context & Analysis

ALMAJECT has 5 FDA actions in our database.

Frequently Asked Questions

How often does ALMAJECT have FDA actions?

ALMAJECT has 5 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 "ANDA065515-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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