RecallHawk

DIAZEPAM (DIAZEPAM ORAL)

CHARTWELL MOLECULAR

Summary

FDA approved DIAZEPAM (DIAZEPAM ORAL) by CHARTWELL MOLECULAR. ANDA (Generic) approval (Labeling) on 2023-01-17. SOLUTION, ORAL.

Details

Source

Drug Approval

External ID

ANDA206477-4

Action Date

2023-01-17

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DIAZEPAM (generic: DIAZEPAM ORAL), SOLUTION, ORAL. Application: ANDA206477

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 "ANDA206477-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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