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NDC 65219-0403-03 Zinc Sulfate 3 mg/mL Details
Zinc Sulfate 3 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 | 65219-0403 |
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Product ID | 65219-403_af258d83-398d-4601-ab09-14c9fe383cc2 |
Associated GPIs | |
GCN Sequence Number | 080056 |
GCN Sequence Number Description | zinc sulfate VIAL 3 MG/ML INTRAVEN |
HIC3 | C3C |
HIC3 Description | ZINC REPLACEMENT |
GCN | 46728 |
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 | 3 |
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 65219-0403-03 (65219040303)
NDC Package Code | 65219-403-03 |
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Billing NDC | 65219040303 |
Package | 25 VIAL in 1 TRAY (65219-403-03) / 10 mL in 1 VIAL (65219-403-01) |
Marketing Start Date | 2022-12-27 |
NDC Exclude Flag | N |
Pricing Information | N/A |