FDA Orange Book
Generic for Accuretic
Accuretic contains quinapril and hydrochlorothiazide. 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 Accuretic is quinapril and hydrochlorothiazide. 2 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
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Accuretic products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| tablet, oral | 12.5MG;EQ 10MG BASE | Discontinued | None | 2 | AB |
| tablet, oral | 12.5MG;EQ 20MG BASE | Discontinued | None | 2 | AB |
| tablet, oral | 25MG;EQ 20MG BASE | Discontinued | None | 2 | AB |
NDA 020125, held by PFIZER PHARMACEUTICALS LTD. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic quinapril and hydrochlorothiazide
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| CHARTWELL RX SCIENCES LLC | 076374 | AB (A-rated, therapeutically equivalent) | March 31, 2004 | 12.5MG;EQ 10MG BASE, 12.5MG;EQ 20MG BASE, 25MG;EQ 20MG BASE |
| AUROBINDO PHARMA LTD | 078450 | AB (A-rated, therapeutically equivalent) | August 24, 2007 | 12.5MG;EQ 10MG BASE, 12.5MG;EQ 20MG BASE, 25MG;EQ 20MG BASE |
Questions
Is there a generic for Accuretic?
Yes. The generic name for Accuretic is quinapril and hydrochlorothiazide. 2 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 Accuretic?
The active ingredient in Accuretic is quinapril and hydrochlorothiazide, 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.