Cupric Chloride 70069-0506
Product NDC
70069-0506- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- May 14, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA216113
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cupric Chloride | .4 mg/mL |
Packaging Options(1)
25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)