NDC 65219-405
Zinc Sulfate
Zinc Sulfate
Zinc Sulfate is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Zinc Sulfate.
| Product ID | 65219-405_af258d83-398d-4601-ab09-14c9fe383cc2 |
| NDC | 65219-405 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Zinc Sulfate |
| Generic Name | Zinc Sulfate |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2022-12-27 |
| Marketing Category | ANDA / |
| Application Number | ANDA216145 |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | ZINC SULFATE |
| Active Ingredient Strength | 5 mg/mL |
| Pharm Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2024-12-31 |