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DELSTRIGO (DORAVIRINE, LAMIVUDINE, AND TENOFOVIR DISOPROXIL FUMARATE)

MSD MERCK CO

Summary

FDA approved DELSTRIGO (DORAVIRINE, LAMIVUDINE, AND TENOFOVIR DISOPROXIL FUMARATE) by MSD MERCK CO. NDA (New Drug) approval (Labeling) on 2025-10-29. TABLET, ORAL.

Details

Source

Drug Approval

External ID

NDA210807-17

Action Date

2025-10-29

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

DELSTRIGO (generic: DORAVIRINE, LAMIVUDINE, AND TENOFOVIR DISOPROXIL FUMARATE), TABLET, ORAL. Application: NDA210807

Context & Analysis

MSD MERCK CO has 3 FDA actions in our database.

Frequently Asked Questions

How often does MSD MERCK CO have FDA actions?

MSD MERCK CO has 3 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 "NDA210807-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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