Zinc Sulfate 70069-0691
Product NDC
70069-0691- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 18, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA216135
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Zinc Sulfate | 5 mg/mL |
Drug Class
Copper Absorption Inhibitor [EPC]Decreased Copper Ion Absorption [PE]
Packaging Options(1)
25 VIAL in 1 CARTON (70069-691-25) / 5 mL in 1 VIAL (70069-691-01)