Cupric Chloride 72603-0351
Product NDC
72603-0351- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217626
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cupric Chloride | .4 mg/mL |
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01)