RecallHawk

METHYLTESTOSTERONE

NOVITIUM PHARMA

Summary

FDA approved METHYLTESTOSTERONE by NOVITIUM PHARMA. ANDA (Generic) approval (Labeling) on 2025-07-11. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA215270-10

Action Date

2025-07-11

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

METHYLTESTOSTERONE, CAPSULE, ORAL. Application: ANDA215270

Context & Analysis

NOVITIUM PHARMA has 23 FDA actions in our database.

Frequently Asked Questions

How often does NOVITIUM PHARMA have FDA actions?

NOVITIUM PHARMA has 23 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 "ANDA215270-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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