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Neutrasaph - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Neutrasaph
Approved
STANDARD
Neutrasaph
Enicar Pharmaceuticals Pvt. Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
2a38d6d99c370029
Company
Enicar Pharmaceuticals Pvt. Ltd.
Type
Standard
Approval Details
Approval Id
2a38d6d99c370029
Drug Approval Philippines Name
Neutrasaph
Product Name
Neutrasaph
Registration Number
DRP-9610
Brand Name
Neutrasaph
Generic Name
Aluminum Hydroxide + Magnesium Hydroxide
Dosage Form
Suspension
Dosage Strength
200mg/100mg per 5mL
Manufacturer
Enicar Pharmaceuticals Pvt. Ltd.
Trader
Sapphire Lifesciences Pvt. Ltd.
Importer
Nelpa Lifesciences, Inc.
Issuance Date
24 March 2021
Expiry Date
24 March 2026
Classification
Over-the-Counter (OTC)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
2a38d6d99c370029
Type
Standard
Back to Philippines FDA Approvals