RecallHawk

LEVETIRACETAM SOLUTION (LEVETIRACETAM)

CHARTWELL MOLECULAR

Summary

FDA approved LEVETIRACETAM SOLUTION (LEVETIRACETAM) by CHARTWELL MOLECULAR. ANDA (Generic) approval (Labeling) on 2026-04-08. SOLUTION, ORAL.

Details

Source

Drug Approval

External ID

ANDA090263-17

Action Date

2026-04-08

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LEVETIRACETAM SOLUTION (generic: LEVETIRACETAM), SOLUTION, ORAL. Application: ANDA090263

Context & Analysis

CHARTWELL MOLECULAR has 19 FDA actions in our database.

Frequently Asked Questions

How often does CHARTWELL MOLECULAR have FDA actions?

CHARTWELL MOLECULAR has 19 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 "ANDA090263-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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