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NDC 65219-0401-01 Zinc Sulfate 1 mg/mL Details
Zinc Sulfate 1 mg/mL
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 Information
| NDC | 65219-0401 |
|---|---|
| Product ID | 65219-401_af258d83-398d-4601-ab09-14c9fe383cc2 |
| Associated GPIs | |
| GCN Sequence Number | 001660 |
| GCN Sequence Number Description | zinc sulfate VIAL 1 MG/ML INTRAVEN |
| HIC3 | C3C |
| HIC3 Description | ZINC REPLACEMENT |
| GCN | 04900 |
| HICL Sequence Number | 000744 |
| HICL Sequence Number Description | ZINC SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | Zinc Sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Zinc Sulfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/mL |
| Substance Name | ZINC SULFATE |
| Labeler Name | Fresenius Kabi USA, LLC |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA216145 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65219-0401-01 (65219040101)
| NDC Package Code | 65219-401-01 |
|---|---|
| Billing NDC | 65219040101 |
| Package | 25 VIAL in 1 TRAY (65219-401-01) / 10 mL in 1 VIAL (65219-401-00) |
| Marketing Start Date | 2022-12-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |