Lofexidine Hydrochloride 72205-0246
Product NDC
72205-0246- Manufacturer
- Novadoz Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 24, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA218699
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lofexidine Hydrochloride | .2 mg/1 |
Packaging Options(2)
1 BOTTLE in 1 CARTON (72205-246-42) / 36 TABLET, FILM COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (72205-246-43) / 96 TABLET, FILM COATED in 1 BOTTLE