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Losarite - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Losarite
Approved
STANDARD
Losarite
Lek Pharmaceuticals d.d
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
e272bf04928f1616
Company
Lek Pharmaceuticals d.d
Type
Standard
Approval Details
Approval Id
e272bf04928f1616
Drug Approval Philippines Name
Losarite
Product Name
Losarite
Registration Number
DRP-2185-03
Brand Name
Losarite
Generic Name
Losartan Potassium + Hydrochlorothiazide
Dosage Form
Film-Coated Tablet
Dosage Strength
50mg/12.5mg
Manufacturer
Lek Pharmaceuticals d.d
Importer
Sandoz Philippines Corporation
Distributor
Ritemed Phils., Inc.
Issuance Date
25 July 2024
Expiry Date
28 October 2029
Pharmacologic Category
Angiotensin II Receptor Blocker/Diuretic
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
e272bf04928f1616
Type
Standard
Back to Philippines FDA Approvals