BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE (BROMPHENIRAMINE MALEATE, PS...
Summary
FDA approved BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE (BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE) by PHARM ASSOC. ANDA (Generic) approval (Labeling) on 2023-05-08. SYRUP, ORAL.
Details
Source
Drug Approval
External ID
ANDA202940-4
Action Date
2023-05-08
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE (generic: BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE), SYRUP, ORAL. Application: ANDA202940
Company
Context & Analysis
PHARM ASSOC has 13 FDA actions in our database.
Frequently Asked Questions
How often does PHARM ASSOC have FDA actions?
PHARM ASSOC 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 "ANDA202940-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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