ACETAMINOPHEN AND CODEINE PHOSPHATE
Summary
FDA approved ACETAMINOPHEN AND CODEINE PHOSPHATE by CHARTWELL MOLECULAR. ANDA (Generic) approval (Labeling) on 2025-12-22. SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
ANDA091238-22
Action Date
2025-12-22
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ACETAMINOPHEN AND CODEINE PHOSPHATE, SOLUTION, ORAL. Application: ANDA091238
Company
Context & Analysis
CHARTWELL MOLECULAR has 19 FDA actions in our database.
Frequently Asked Questions
How often does CHARTWELL MOLECULAR have FDA actions?
CHARTWELL MOLECULAR has 19 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 "ANDA091238-22" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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