RecallHawk

BUPIVACAINE

HENGRUI PHARMA

Summary

FDA approved BUPIVACAINE by HENGRUI PHARMA. ANDA (Generic) approval on 2024-07-01. INJECTABLE, LIPOSOMAL, INJECTION.

Details

Source

Drug Approval

External ID

ANDA214348-1

Action Date

2024-07-01

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BUPIVACAINE, INJECTABLE, LIPOSOMAL, INJECTION. Application: ANDA214348

Context & Analysis

HENGRUI PHARMA has 6 FDA actions in our database.

Frequently Asked Questions

How often does HENGRUI PHARMA have FDA actions?

HENGRUI PHARMA has 6 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 "ANDA214348-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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