METHADONE HYDROCHLORIDE
Summary
FDA approved METHADONE HYDROCHLORIDE by VISTAPHARM LLC. ANDA (Generic) approval (Labeling) on 2024-08-27. TABLET, FOR SUSPENSION, ORAL.
Details
Source
Drug Approval
External ID
ANDA075082-17
Action Date
2024-08-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
METHADONE HYDROCHLORIDE, TABLET, FOR SUSPENSION, ORAL. Application: ANDA075082
Company
Context & Analysis
VISTAPHARM LLC has 11 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
How often does VISTAPHARM LLC have FDA actions?
VISTAPHARM LLC has 11 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA075082-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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