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MYLAN-EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE - Health Canada Drug Approval Details
Approvals
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Health Canada
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MYLAN-EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE
Authorized
STANDARD
MYLAN-EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE
Mylan Pharmaceuticals ULC
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
752c431964b407c0
Company
Mylan Pharmaceuticals ULC
Type
Standard
Approval Details
Approval Id
752c431964b407c0
Drug Approval Canada Name
MYLAN-EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE
Product Name
MYLAN-EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE
Status
Marketed
Status Date
2017-07-31
Original Market Date
2017-07-31
Din
02461412
Drug Class
Human
Dosage Form
Tablet
Route Of Administration
Oral
Schedule
Prescription
Ahfs
08:18.08.16
Atc Original
J05AR06 EMTRICITABINE, TENOFOVIR DISOPROXIL AND EFAVIRENZ
Atc Name
j 05 ar 06
Aig Number
0352327001
Company Name
Mylan Pharmaceuticals ULC
Company Address
85 Advance Road, Etobicoke, Ontario, Canada, M8Z 2S6
Active Ingredients
EFAVIRENZ
600 MG
TENOFOVIR DISOPROXIL FUMARATE
300 MG
EMTRICITABINE
200 MG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
752c431964b407c0
Type
Standard
Back to Health Canada Approvals