S0003658

EFV600mg+FTC200mg+TDF300mg tabs/PAC-30


Efavirenz 600mg + Emtricitabine 200mg + Tenofovir disoproxil fumarate 300mg, (equivalent to 245mg Tenofovir disoproxil), film coated tablets, bottle pack of 30
Indicative Price : Upon Request

NOTE: The description below is for a standard product. It is not specific to patent status and pricing policies that may apply at country level. This information is available on request from Supply Division: Contact: supply@unicef.org

General Description:
Efavirenz 600mg + Emtricitabine 200mg + Tenofovir Disoproxil Fumarate 300mg, equivalent to 245mg Tenofovir Disoproxil, film coated tablet, pack of 30 tablets

Technical Specifications:
Each film coated tablet contains Efavirenz 600mg and Emtricitabine 200mg and Tenofovir Disoproxil Fumarate 300mg, equivalent to 245mg Tenofovir Disoproxil as fixed dose combination.

Therapeutic class:
Efavirenz is a Non Nucleoside Reverse Transcriptase Inhibitor (NNRTI)
Emtricitabine is a Nucleoside Reverse Transcriptase Inhibitor (NRTI)
Tenofovir is a Nucleotide Reverse Transcriptase Inhibitor (NtRTI)

Standard shelf life:
2 years (24 months)

Other available formulations:
The product may also be available in other formulations, pack sizes, or in combinations with other ARVs.

Guidelines for use:
For more details, please click the links listed below:

WHO treatment guidelines


and

WHO Essential Medicines Library


or your regional national guidelines

For details about paediatric dosage schemes, please click the links listed below:

WHO HIV/AIDS


WHO Generic tool for assessing paediatric ARV dosing


Indications:
Management of HIV-1 infection in adults as a complete regimen or in combination with other antiretroviral drugs. By mouth (oral) PO.

Storage:
Store below 30ºC (86ºF), in a tightly closed container.
Pack should come with desiccant
Keep out of reach and sight of children.

Dispensing instructions:
Dispense in original container. Do not repack.
To be taken on an empty stomach.
Advise patient to take the medicine at bedtime especially in the first 2-4 weeks to reduce CNS side effects.

Regulatory Status:
For latest updates, please click the links listed below:

List of WHO Prequalified Medicines


List of USFDA approved and tentatively approved items



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