DYE FREE IBUPROFEN (IBUPROFEN)
Summary
FDA approved DYE FREE IBUPROFEN (IBUPROFEN) by LNK. ANDA (Generic) approval (Manufacturing (CMC)) on 2025-03-20. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA075139-18
Action Date
2025-03-20
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DYE FREE IBUPROFEN (generic: IBUPROFEN), TABLET, ORAL. Application: ANDA075139
Company
Context & Analysis
Frequently Asked Questions
How often does LNK have FDA actions?
This is the only FDA action we have on record for LNK in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA075139-18" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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