RecallHawk

FOSAMPRENAVIR CALCIUM

SUN PHARM

Summary

FDA approved FOSAMPRENAVIR CALCIUM by SUN PHARM. ANDA (Generic) approval (Labeling) on 2025-04-22. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA204024-9

Action Date

2025-04-22

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

FOSAMPRENAVIR CALCIUM, TABLET, ORAL. Application: ANDA204024

Company

Context & Analysis

SUN PHARM has 48 FDA actions in our database.

Frequently Asked Questions

How often does SUN PHARM have FDA actions?

SUN PHARM has 48 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 "ANDA204024-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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