RecallHawk

ISTODAX (ROMIDEPSIN)

BRISTOL-MYERS

Summary

FDA approved ISTODAX (ROMIDEPSIN) by BRISTOL-MYERS. NDA (New Drug) approval (Efficacy) on 2021-07-30. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA022393-17

Action Date

2021-07-30

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

ISTODAX (generic: ROMIDEPSIN), POWDER, INTRAVENOUS. Application: NDA022393

Context & Analysis

BRISTOL-MYERS has 4 FDA actions in our database.

Frequently Asked Questions

How often does BRISTOL-MYERS have FDA actions?

BRISTOL-MYERS has 4 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 "NDA022393-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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