RecallHawk

Summary

FDA approved PROPOFOL by SAGENT PHARMS INC. ANDA (Generic) approval (Labeling) on 2025-08-12. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA075102-46

Action Date

2025-08-12

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

PROPOFOL, INJECTABLE, INJECTION. Application: ANDA075102

Context & Analysis

SAGENT PHARMS INC has 18 FDA actions in our database.

Frequently Asked Questions

How often does SAGENT PHARMS INC have FDA actions?

SAGENT PHARMS INC has 18 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 "ANDA075102-46" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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