AEGiS-FDA: Tentative approval: generic Abacavir Sulfate Oral Solution Food and Drug AdministrationImportant note: Information in this article was accurate in 2006. The state of the art may have changed since the publication date.
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Tentative approval: generic Abacavir Sulfate Oral Solution

Food and Drug Administration - June 28, 2006
Richard Klein


The Food and Drug Administration, on June 27, 2006, granted tentative approval for Abacavir Sulfate Oral Solution, 20 mg/mL, manufactured by Aurobindo Pharma Limited Inc., of Hyderabad, India.

This is a generic version of the already-approved Ziagen brand of the product manufactured by GlaxoSmithKline .

The application was reviewed under expedited review provisions for the President's Emergency Plan for AIDS Relief (PEPFAR).

"Tentative Approval" means that FDA has concluded that a drug product has met all required quality, safety and efficacy standards, though it may not yet be marketed in the U.S. because of existing patents and/or exclusivity rights. Tentative approval, however, does make the product eligible for consideration for purchase under the PEPFAR program.

Abacavir sulfate is a member of the class of drugs known as nucleoside reverse transcriptase inhibitors (NRTIs), which help keep the AIDS virus from reproducing. This antiretroviral drug is intended to be used in combination with other antiretroviral agents for the treatment of HIV-1 infection.

Richard Klein, Office of Special Health Issues

Food and Drug Administration
060628
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SOURCE: Food and Drug Administration (FDA).

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