CHILDRENS IBUPROFEN ORAL SUSPENSION (IBUPROFEN)
Summary
FDA approved CHILDRENS IBUPROFEN ORAL SUSPENSION (IBUPROFEN) by PAI HOLDINGS PHARM. ANDA (Generic) approval on 2024-11-08. SUSPENSION, ORAL.
Details
Source
Drug Approval
External ID
ANDA214789-1
Action Date
2024-11-08
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CHILDRENS IBUPROFEN ORAL SUSPENSION (generic: IBUPROFEN), SUSPENSION, ORAL. Application: ANDA214789
Company
Context & Analysis
PAI HOLDINGS PHARM has 2 FDA actions in our database.
Frequently Asked Questions
How often does PAI HOLDINGS PHARM have FDA actions?
PAI HOLDINGS PHARM has 2 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 "ANDA214789-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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