ACETAMINOPHEN AND CODEINE PHOSPHATE
Summary
FDA approved ACETAMINOPHEN AND CODEINE PHOSPHATE by RHODES PHARMS. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA089673-34
Action Date
2026-06-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ACETAMINOPHEN AND CODEINE PHOSPHATE, TABLET, ORAL. Application: ANDA089673
Company
Context & Analysis
RHODES PHARMS has 13 FDA actions in our database.
Frequently Asked Questions
How often does RHODES PHARMS have FDA actions?
RHODES PHARMS has 13 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 "ANDA089673-34" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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