FDA Orange Book
Generic for Epzicom
Epzicom contains abacavir and lamivudine. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.
Source: FDA Orange Book data file dated 2026-10-09. Publisher page
Yes. The generic name for Epzicom is abacavir and lamivudine. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
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Epzicom products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| tablet, oral | EQ 600MG BASE;300MG | Discontinued | None | 5 | AB |
NDA 021652, held by VIIV HEALTHCARE CO. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic abacavir and lamivudine
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| CHARTWELL RX SCIENCES LLC | 204990 | AB (A-rated, therapeutically equivalent) | March 28, 2017 | EQ 600MG BASE;300MG |
| CIPLA LTD | 091144 | AB (A-rated, therapeutically equivalent) | March 28, 2017 | EQ 600MG BASE;300MG |
| AUROBINDO PHARMA LTD | 090159 | AB (A-rated, therapeutically equivalent) | November 15, 2018 | EQ 600MG BASE;300MG |
| LAURUS LABS LTD | 216332 | AB (A-rated, therapeutically equivalent) | July 25, 2022 | EQ 600MG BASE;300MG |
| HETERO LABS LTD UNIT V | 205412 | AB (A-rated, therapeutically equivalent) | April 16, 2025 | EQ 600MG BASE;300MG |
Questions
Is there a generic for Epzicom?
Yes. The generic name for Epzicom is abacavir and lamivudine. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
What is the generic name for Epzicom?
The active ingredient in Epzicom is abacavir and lamivudine, per the FDA Orange Book.
What does a therapeutic equivalence code mean?
In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.