RecallHawk

MORPHINE SULFATE

WINDER LABS LLC

Summary

FDA approved MORPHINE SULFATE by WINDER LABS LLC. ANDA (Generic) approval (REMS) on 2026-06-18. SOLUTION, ORAL.

Details

Source

Drug Approval

External ID

ANDA211454-4

Action Date

2026-06-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MORPHINE SULFATE, SOLUTION, ORAL. Application: ANDA211454

Context & Analysis

WINDER LABS LLC has 2 FDA actions in our database.

Frequently Asked Questions

How often does WINDER LABS LLC have FDA actions?

WINDER LABS LLC has 2 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 "ANDA211454-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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