RecallHawk

EGRIFTA WR (TESAMORELIN)

THERATECHNOLOGIES

Summary

FDA approved EGRIFTA WR (TESAMORELIN) by THERATECHNOLOGIES. BLA (Biologic) approval (Manufacturing (CMC)) on 2025-03-25. POWDER, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

BLA022505-20

Action Date

2025-03-25

Status

Approved

Category

drug

Product Code

BLA (Biologic)

Product Description

EGRIFTA WR (generic: TESAMORELIN), POWDER, SUBCUTANEOUS. Application: BLA022505

Context & Analysis

THERATECHNOLOGIES has 2 FDA actions in our database.

Frequently Asked Questions

How often does THERATECHNOLOGIES have FDA actions?

THERATECHNOLOGIES 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 "BLA022505-20" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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