RecallHawk

METHADONE HYDROCHLORIDE

SPECGX LLC

Summary

FDA approved METHADONE HYDROCHLORIDE by SPECGX LLC. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA040517-42

Action Date

2026-06-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

METHADONE HYDROCHLORIDE, TABLET, ORAL. Application: ANDA040517

Company

Context & Analysis

SPECGX LLC has 19 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

How often does SPECGX LLC have FDA actions?

SPECGX LLC has 19 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA040517-42" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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