Lofexidine hydrochloride .2 mg/1
lofexidine hydrochloride · TABLET, FILM COATED · Prasco Laboratories
No Recall History
Plain English
Lofexidine hydrochloride is a tablet, film coated containing lofexidine hydrochloride at .2 mg/1, taken oral. Manufactured by Prasco Laboratories.
Key Facts
- Brand Name
- Lofexidine hydrochloride
- Generic Name
- lofexidine hydrochloride
- NDC Code (Product)
66993-345- Manufacturer
- Prasco Laboratories
- Strength
- .2 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA209229
- Marketing Start
- 08/29/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Lofexidine hydrochloride used for?
Lofexidine hydrochloride contains lofexidine hydrochloride. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Lofexidine hydrochloride a controlled substance?
Lofexidine hydrochloride is not classified as a controlled substance by the DEA.
What is the generic name for Lofexidine hydrochloride?
The generic name for Lofexidine hydrochloride is lofexidine hydrochloride. There are 2 other brand versions of lofexidine hydrochloride.
What is the NDC code for Lofexidine hydrochloride .2 mg/1?
The NDC (National Drug Code) for Lofexidine hydrochloride .2 mg/1 is 66993-345, listed by Prasco Laboratories.