HEMICLOR (CHLORTHALIDONE)
Summary
FDA approved HEMICLOR (CHLORTHALIDONE) by PRM PHARMA. NDA (New Drug) approval (Type 3 - New Dosage Form) on 2025-03-17. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA218647-1
Action Date
2025-03-17
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
HEMICLOR (generic: CHLORTHALIDONE), TABLET, ORAL. Application: NDA218647
Company
Context & Analysis
Frequently Asked Questions
How often does PRM PHARMA have FDA actions?
This is the only FDA action we have on record for PRM PHARMA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA218647-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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