Strength
.2 mg/1
Manufacturer
USWM, LLCNDC
78670005036
Classification
Brand
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
11/19/2025
Active Ingredients
LOFEXIDINE HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA209229On Market Since
2/9/2021
Related Drugs
Same classification
No related drugs found.