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Approvals
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Philippines FDA
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Aluzet
Approved
STANDARD
Aluzet
Sapphire Lifesciences Pvt. Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
193e527358586093
Company
Sapphire Lifesciences Pvt. Ltd.
Type
Standard
Approval Details
Approval Id
193e527358586093
Drug Approval Philippines Name
Aluzet
Product Name
Aluzet
Registration Number
DRP-4115-01
Brand Name
Aluzet
Generic Name
Aluminum Hydroxide+ Magnesium Hydroxide
Dosage Form
Chewable Tablet
Dosage Strength
200 mg/ 100 mg
Manufacturer
Sapphire Lifesciences Pvt. Ltd.
Importer
Nelpa Lifesciences, Inc.
Distributor
777 Red Pharma Inc.
Issuance Date
29 November 2022
Expiry Date
23 November 2027
Pharmacologic Category
Antacid
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
193e527358586093
Type
Standard
Back to Philippines FDA Approvals
Aluzet - Philippines FDA Drug Approval Details