PROCHLORPERAZINE EDISYLATE
Summary
FDA approved PROCHLORPERAZINE EDISYLATE by VIWIT PHARM. ANDA (Generic) approval (Labeling) on 2023-04-07. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA213626-1
Action Date
2023-04-07
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
PROCHLORPERAZINE EDISYLATE, INJECTABLE, INJECTION. Application: ANDA213626
Company
Context & Analysis
VIWIT PHARM has 5 FDA actions in our database.
Frequently Asked Questions
How often does VIWIT PHARM have FDA actions?
VIWIT PHARM has 5 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 "ANDA213626-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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