ACCURETIC® How Supplied/Storage and Handling (quinapril HCl, hydrochlorothiazide)

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HOW SUPPLIED

ACCURETIC is available in tablets of three different strengths:

10/12.5 tablets: pink, scored elliptical, biconvex, film-coated tablets coded "PD 222" on one side. Each tablet contains 10 mg of quinapril and 12.5 mg of hydrochlorothiazide.

NDC 0071-3112-23: 90 tablet bottles

20/12.5 tablets: pink, scored triangular, film-coated tablets coded "PD 220" on one side. Each tablet contains 20 mg of quinapril and 12.5 mg of hydrochlorothiazide.

NDC 0071-5212-23: 90 tablet bottles

20/25 tablets: pink, round, biconvex, film-coated tablets coded "PD 223" on one side. Each tablet contains 20 mg of quinapril and 25 mg of hydrochlorothiazide.

NDC 0071-7225-23: 90 tablet bottles

Dispense in tight containers as defined in the USP.

Store at Controlled Room Temperature 20–25°C (68–77°F) [see USP].

If you provide additional keywords, you may be able to browse through our database of Scientific Response Documents.

Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.

ACCURETIC® Quick Finder

Availability

Pfizer is experiencing a supply shortage of Accuretic because of manufacturing disruptions. While Pfizer is managing this situation with urgency, at this time, we are unable to confirm a date when the situation will be resolved.

We understand and regret the challenges that this situation poses to patients. Pfizer fully realizes the importance of this medicine to patients. Ensuring continuity of the supply of our medicines is paramount. Until the Accuretic shortage is resolved, patients will need to consult with their healthcare professional to choose an alternate treatment option.

Please refer to the full Prescribing Information on important treatment considerations for Accuretic via the following link In the event this link does not work, please access the product’s approved Prescribing Information at www.pfizer.com/products.
Report an adverse event or concern about the quality of a Pfizer product

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*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

If you cannot use the above website to report an adverse event related to a Pfizer product, please call Pfizer Medical Information at (800) 438-1985.

If you prefer, you may contact the U.S. Food and Drug Administration (FDA) directly by visiting www.fda.gov/medwatch or by calling (800)-332-1088.
Assistance programs (for eligible patients)

Pfizer RxPathways connects eligible patients to a range of assistance programs that offer insurance support, co-pay help, and medicines for free or at a savings. Patients and physicians can contact RxPathways at (866) 706-2400 or visit the website for more information on these programs www.pfizerrxpathways.com.
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