Strength
.2 mg/1
Manufacturer
Prasco LaboratoriesNDC
66993034576
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LOFEXIDINE HYDROCHLORIDEApproval Type
Authorized Generic (NDA)
FDA Application
NDA209229On Market Since
8/29/2024
Related Drugs
Same classification
No related drugs found.