Lofexidine 71921-0250
Product NDC
71921-0250- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 21, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA218613
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lofexidine Hydrochloride | .18 mg/1 |
Packaging Options(2)
1 BOTTLE in 1 CARTON (71921-250-36) / 36 TABLET, COATED in 1 BOTTLE
1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE