RecallHawk

ENOXAPARIN SODIUM

SANOFI AVENTIS US

Summary

FDA approved ENOXAPARIN SODIUM by SANOFI AVENTIS US. NDA (New Drug) approval (Labeling) on 2023-07-28. INJECTABLE, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

NDA020164-101

Action Date

2023-07-28

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

ENOXAPARIN SODIUM, INJECTABLE, SUBCUTANEOUS. Application: NDA020164

Context & Analysis

SANOFI AVENTIS US has 14 FDA actions in our database.

Frequently Asked Questions

How often does SANOFI AVENTIS US have FDA actions?

SANOFI AVENTIS US has 14 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 "NDA020164-101" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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