Lofexidine 70954-0909
Product NDC
70954-0909- Manufacturer
- Ani Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 22, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA219917
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lofexidine Hydrochloride | .18 mg/1 |
Packaging Options(2)
36 TABLET in 1 BOTTLE (70954-909-10)
96 TABLET in 1 BOTTLE (70954-909-20)