Lofexidine Hydrochloride 66993-0345
Product NDC
66993-0345- Manufacturer
- Prasco Laboratories
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 29, 2024
- Listing Expires
- December 31, 2026
- Application
- NDA209229
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lofexidine Hydrochloride | .2 mg/1 |
Packaging Options(2)
1 BOTTLE in 1 CARTON (66993-345-37) / 36 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE