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HOVID TENOFOVIR DISOPROXIL FUMARATE TABLETS 300MG - PPB Drug Approval Details
Approvals
/
PPB
/
HOVID TENOFOVIR DISOPROXIL FUMARATE TABLETS 300MG
Approved
STANDARD
HOVID TENOFOVIR DISOPROXIL FUMARATE TABLETS 300MG
HOVID LIMITED
🇰🇪 Pharmacy and Poisons Board
Approval Date
Jun 21, 2024
Approval ID
6d20d9725388e601
Company
HOVID LIMITED
Type
Standard
Approval Details
Approval Id
6d20d9725388e601
Product Name
HOVID TENOFOVIR DISOPROXIL FUMARATE TABLETS 300MG
Drug Hk Name
HOVID TENOFOVIR DISOPROXIL FUMARATE TABLETS 300MG
Registration Code
HK-67561
Company Name
HOVID LIMITED
Company Detail Path
/organization/hovid-limited
Registration Category
Part 1, Schedule 1 & Schedule 3 Poison
Sale Requirement
Prescription only Medicines
Registration Date
2022-09-13
Company Address
FLAT/RM 07, 18/F., PACIFIC PLAZA, 410 DES VOEUX ROAD WEST, HONG KONG
Active Ingredients
Approved
Quick Info
Agency
PPB
Country
🇰🇪
Approval Date
Jun 21, 2024
Approval ID
6d20d9725388e601
Type
Standard
Back to PPB Approvals