Strength
.18 mg/1
Manufacturer
Florida Pharmaceutical Products, LLCNDC
71921025096
Classification
Generic
Dosage Form
TABLET, COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LOFEXIDINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA218613On Market Since
8/21/2024
Related Drugs
Same classification
No related drugs found.