Quinapril may cause a rare reaction called angioedema, where there is swelling under the skin. This medicine should not be used if you have had angioedema. Drug Interactions.

Quinapril(Accupril) generic is an angiotensin-converting enzyme (ACE) inhibitor, prescribed for high blood pressure and heart failure either alone or with other medications.

Quinapril was well tolerated, and the incidence of adverse events was comparable with or less than that of captopril or enalapril. In the study of Paolisso et al., ...

Lupin Pharmaceuticals Inc.’s Quinapril tablets, sold in 20 mg and 40 mg, may contain an elevated level of nitrosamine impurity, N-Nitroso-Quinapril, above the acceptable daily intake level.

The recalled lot of Quinapril Tablets USP 20mg; NDC Number 68180-558-09; Lot Number G102929; Exp Date 4/2023, is supplied in 90-count bottles.

The recall involves Quinapril and Hydrochlorothiazide Tablets USP, 20mg / 12.5mg, supplied in 90's HDPE bottle, with lot code QE2021005-A and QE2021010-A, and expiry of 01/2023.

How to Take Quinapril and it's Dose Written by - Dhanalakshmi Chinnuswamy, Diploma in Pharmacy, MBA (Healthcare) Medically Checked by - Dr. M. Janani Priya, Doctor of Pharmacy ...

Quinapril is prescribed to around a million Americans each year to treat hypertension and heart failure. However, testing at various sites found excessive amounts of nitrosamine in the pills.

The recall concerns lot Nos. QE2021005-A and QE2021010-A of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg in 90-count bottles from Aurobindo Pharma with an expiration date of ...

The recall concerns lot Nos. QE2021005-A and QE2021010-A of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg in 90-count bottles from Aurobindo Pharma with an expiration date of ...

The Quinapril tablet USP under the Lupin Quinapril tablets recall is considered to be an angiotensin-converting enzyme (ACE) inhibitor, which is used to treat hypertension and lower blood pressure.

More Quinapril and Hydrochlorothiazide Tablets USP in 20 mg and 12.5 mg doses, respectively. And the contaminant is Nitrosamine Drug Substance Related Impurity (NDSRI), ...