HYDROXYCHLOROQUINE SULFATE
Summary
FDA approved HYDROXYCHLOROQUINE SULFATE by ALKALOIDA ZRT. ANDA (Generic) approval (Labeling) on 2024-08-27. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA201691-8
Action Date
2024-08-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
HYDROXYCHLOROQUINE SULFATE, TABLET, ORAL. Application: ANDA201691
Company
Context & Analysis
Frequently Asked Questions
How often does ALKALOIDA ZRT have FDA actions?
This is the only FDA action we have on record for ALKALOIDA ZRT in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA201691-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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