BENAZEPRIL HYDROCHLORIDE
Generic: BENAZEPRIL HYDROCHLORIDE
Solco healthcare U.S.Manufacturer
ORALRoute
BENAZEPRIL HYDROCHLORIDEActive Substance
2004-02-11Original Approval
BENAZEPRIL HYDROCHLORIDE is FDA application ANDA076118, sponsored by PRINSTON INC. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Recalls
Class II2025-07-02
Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin PharmaceuLabeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 inst
Class II2012-04-09
Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd. By: Dr. Reddy's LAdulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabe
Class III2019-09-24
Benazepril HCl Tablets, USP 40 mg, 100 count bottles, Rx only, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ NPresence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle
Top Reported Reactions
1
FATIGUE
293 reports
2
NAUSEA
261 reports
3
DIARRHOEA
257 reports
4
DRUG INEFFECTIVE
248 reports
5
HEADACHE
239 reports
6
DYSPNOEA
231 reports
7
DIZZINESS
223 reports
8
PAIN
214 reports
9
ASTHENIA
178 reports
10
PRURITUS
174 reports