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Nofoxil Tenofovir Disoproxil Fumarate Tablet 300mg 30tablets for Anti HIV

Basic Info

Model No.:  Anti-HIV004

Product Description

Model NO.: Anti-HIV004 Usage Mode: For oral administration State: Solid Type: Biological Products OEM: Acceptable Specification: Tenofovir Disoproxil Fumarate 300mg HS Code: 2923900090 Application: Internal Medicine Suitable for: Elderly, Adult Shape: Tablet Pharmaceutical Technology: Chemical Synthesis Trademark: GUYENNE Origin: France Product Description
Nofoxil Tenofovir Disoproxil Fumarate Tablet 300mg 30tablets for Anti HIV
Specification 300mg
Package 30tablets/bottle

Tenofovir disoproxil is an antiretroviral medication used to prevent and treat HIV/AIDS and to treat chronic hepatitis B. The active substance is tenofovir, while tenofovir disoproxil is a prodrug that is used because of its better absorption in the gut.

Medical uses
Tenofovir disoproxil fumarate (tenofovir DF) is a bioavailable prodrug of tenofovir, a potent nucleotide analogue reverse-transcriptase inhibitor with activity against human immunodeficiency virus (HIV) and hepatitis B virus. It is administered as a single 300-mg tablet once daily. It was approved for the treatment of HIV infection on the basis of data from clinical trials demonstrating activity in treatment-experienced patients, and it was subsequently shown to be effective when used as a component of initial therapy. Tenofovir DF is active against some nucleoside-resistant strains of HIV. However, cross-resistance is associated with multiple thymidine analogue mutations that include 41L or 210W. The signature mutation is the K65R mutation, which causes variable loss in susceptibility to tenofovir DF, . Tenofovir DF has been well tolerated in clinical trials with durations of follow-up up to 96 weeks. It is associated with more-favorable lipid profiles than and has not been associated with the mitochondrial toxicity attributed to other nucleoside analogues.

Tenofovir disoproxil fumarate (tenofovir DF) is an orally bioavailable prodrug of tenofovir. It is the first nucleotide analogue reverse-transcriptase inhibitor (NtRTI) to have been approved by the US Food and Drug Administration (FDA) for the treatment of HIV infection. Since its approval in October 2001, this analogue of adenine 5′ monophosphate has quickly become a widely used component of antiretroviral regimens for both treatment-naive and -experienced patients on the basis of its efficacy and tolerability in several clinical trials.

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Product Categories : Anti-Hiv Drug

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