RecallHawk

REMIFENTANIL HYDROCHLORIDE

NIVAGEN PHARMS INC

Summary

FDA approved REMIFENTANIL HYDROCHLORIDE by NIVAGEN PHARMS INC. ANDA (Generic) approval on 2024-06-28. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA215635-1

Action Date

2024-06-28

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

REMIFENTANIL HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA215635

Context & Analysis

Frequently Asked Questions

How often does NIVAGEN PHARMS INC have FDA actions?

This is the only FDA action we have on record for NIVAGEN PHARMS INC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA215635-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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