RecallHawk

SAPROPTERIN DIHYDROCHLORIDE

HIKMA

Summary

FDA approved SAPROPTERIN DIHYDROCHLORIDE by HIKMA. ANDA (Generic) approval on 2025-06-11. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA218797-1

Action Date

2025-06-11

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

SAPROPTERIN DIHYDROCHLORIDE, TABLET, ORAL. Application: ANDA218797

Company

Context & Analysis

HIKMA has 117 FDA actions in our database.

Frequently Asked Questions

How often does HIKMA have FDA actions?

HIKMA has 117 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 "ANDA218797-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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