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Saphmox 500 - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Saphmox 500
Approved
STANDARD
Saphmox 500
Sunlovis Pharmaceuticals LLP
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
0a09bf4ca6b2bccb
Company
Sunlovis Pharmaceuticals LLP
Type
Standard
Approval Details
Approval Id
0a09bf4ca6b2bccb
Drug Approval Philippines Name
Saphmox 500
Product Name
Saphmox 500
Registration Number
DRP-8388
Brand Name
Saphmox 500
Generic Name
Amoxicillin (as Trihydrate)
Dosage Form
Capsule
Dosage Strength
500mg
Manufacturer
Sunlovis Pharmaceuticals LLP
Trader
Sapphire Lifesciences Pvt. Ltd.
Importer
Nelpa Lifesciences, Inc.
Distributor
Nelpa Lifesciences, Inc.
Issuance Date
27 December 2022
Expiry Date
04 August 2026
Pharmacologic Category
Antibacterial (Penicillin)
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
0a09bf4ca6b2bccb
Type
Standard
Back to Philippines FDA Approvals