ADVIL (IBUPROFEN SODIUM)
Summary
FDA approved ADVIL (IBUPROFEN SODIUM) by HALEON US HOLDINGS. NDA (New Drug) approval (Labeling) on 2022-02-08. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA201803-16
Action Date
2022-02-08
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ADVIL (generic: IBUPROFEN SODIUM), TABLET, ORAL. Application: NDA201803
Company
Context & Analysis
HALEON US HOLDINGS has 10 FDA actions in our database.
Frequently Asked Questions
How often does HALEON US HOLDINGS have FDA actions?
HALEON US HOLDINGS has 10 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 "NDA201803-16" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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