ZOLPIDEM TARTRATE
Summary
FDA approved ZOLPIDEM TARTRATE by CHARTWELL MOLECULAR. ANDA (Generic) approval (Labeling) on 2022-09-28. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA077388-5
Action Date
2022-09-28
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ZOLPIDEM TARTRATE, TABLET, ORAL. Application: ANDA077388
Company
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 "ANDA077388-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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