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SILDERA TABLETS 50MG - PPB Drug Approval Details
Approvals
/
PPB
/
SILDERA TABLETS 50MG
Approved
STANDARD
SILDERA TABLETS 50MG
ATLANTIC PHARMACEUTICAL LIMITED
🇰🇪 Pharmacy and Poisons Board
Approval Date
Sep 17, 2025
Approval ID
f3a7df67bb59d283
Company
ATLANTIC PHARMACEUTICAL LIMITED
Type
Standard
Approval Details
Approval Id
f3a7df67bb59d283
Product Name
SILDERA TABLETS 50MG
Drug Hk Name
SILDERA TABLETS 50MG
Registration Code
HK-68783
Company Name
ATLANTIC PHARMACEUTICAL LIMITED
Company Detail Path
/organization/atlantic-pharmaceutical-limited
Registration Category
Part 1, Schedule 1 & Schedule 3 Poison
Sale Requirement
Prescription only Medicines
Registration Date
2025-07-31
Company Address
18/F, BLK A, WING WAH IND BLDG, 677 KING'S RD, NORTH POINT, HONG KONG
Active Ingredients
Approved
Quick Info
Agency
PPB
Country
🇰🇪
Approval Date
Sep 17, 2025
Approval ID
f3a7df67bb59d283
Type
Standard
Back to PPB Approvals