FDA approval of generic ARVs

Since the last issue of HTB, the US Food and Drug Administration (FDA) has granted tentative approval for the following new generic ARV products.

Date Drug Company
9 May 2008 FTC (emtricitabine) Aurobindo, India
25 March 2008 AZT (300mg) Hetero, India
25 March 2008 AZT+3TC (300/150mg) Hetero, India
20 March 2008 d4T (30mg) + 3TC + nevirapine Strides, India
20 March 2008 d4T (40mg) + 3TC + nevirapine Strides, India

“Tentative Approval” means that FDA has concluded that a drug product has met all required quality, safety and efficacy standards, but because of existing patents and/or exclusivity rights, it cannot yet be marketed in the United States. Tentative approval does, however make the product eligible for consideration for purchase under the PEPFAR program for use outside the United States.

Effective patent dates are listed in the agency’s publication titled Approved Drug Products with Therapeutic Equivalence Evaluations, also known as the also known as the Orange Book.


This brings the total of FDA approved generic drugs and formulations to 67 since the programme started.

Updated list of generic tentative approvals:

Source: FDA list serve:

An archive of past list serve announcements is available on the FDA web site:

Links to other websites are current at date of posting but not maintained.