ACCURETIC® Principal Display Panel (quinapril HCl, hydrochlorothiazide)

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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.

PRINCIPAL DISPLAY PANEL - 20 mg/25 mg Tablet Bottle Label

Pfizer

NDC 0071-0223-23

Accuretic™
(quinapril HCl/
hydrochlorothiazide)
Tablets

20 mg/25 mg*

90 Tablets
Rx only

PRINCIPAL DISPLAY PANEL - 10 mg/12.5 mg Tablet Bottle Label - NDC 0071-3112-23

Pfizer

NDC 0071-3112-23

Accuretic™
(quinapril and
hydrochlorothiazide)
tablets

10 mg/12.5 mg*

90 Tablets
Rx only

PRINCIPAL DISPLAY PANEL - 20 mg/12.5 mg Tablet Bottle Label - NDC 0071-5212-23

Pfizer

NDC 0071-5212-23

Accuretic™
(quinapril and
hydrochlorothiazide)
tablets

20 mg/12.5 mg*

90 Tablets
Rx only

PRINCIPAL DISPLAY PANEL - 20 mg/25 mg Tablet Bottle Label - NDC 0071-7225-23

Pfizer

NDC 0071-7225-23

Accuretic™
(quinapril and
hydrochlorothiazide)
tablets

20 mg/25 mg*

90 Tablets
Rx only

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

To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, click the link below to submit your information:
Pfizer Safety Reporting Site
*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 or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety 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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