CUPRIC SULFATE
Summary
FDA approved CUPRIC SULFATE by APOTEX CORP. ANDA (Generic) approval on 2024-08-19. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA218745-1
Action Date
2024-08-19
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CUPRIC SULFATE, INJECTABLE, INJECTION. Application: ANDA218745
Company
Context & Analysis
APOTEX CORP has 19 FDA actions in our database, including 18 recalls.
Frequently Asked Questions
How often does APOTEX CORP have FDA actions?
APOTEX CORP has 19 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA218745-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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