Goprelto 70839-0359
Generic: Cocaine Hydrochloride
Product NDC
70839-0359- Manufacturer
- Lxo Us Inc.
- Dosage Form
- Solution
- Route
- Nasal
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CII
- Marketing Start
- February 9, 2024
- Listing Expires
- December 31, 2026
- Application
- NDA209963
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cocaine Hydrochloride | 40 mg/mL |
Packaging Options(1)
1 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASS