FELODIPINE

Generic: FELODIPINE

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.Manufacturer
ORALRoute
FELODIPINEActive Substance
2013-11-08Original Approval

FELODIPINE is FDA application ANDA201964, sponsored by HERITAGE. 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 III2020-10-23
Felodipine Extended Release Tablets, USP 10 mg,100-count bottle, Rx only, Distributed by: Heritage Pharmaceuticals Inc.

Failed impurities/ degradation specifications: Out of specification impurity results were observed d

Top Reported Reactions

1
FATIGUE
1,109 reports
2
DYSPNOEA
1,001 reports
3
DIZZINESS
1,000 reports
4
DIARRHOEA
887 reports
5
NAUSEA
887 reports
6
HEADACHE
883 reports
7
PAIN
852 reports
8
PYREXIA
782 reports
9
VOMITING
736 reports
10
MALAISE
698 reports