Package 65219-401-01

Brand: zinc sulfate

Generic: zinc sulfate
NDC Package

Package Facts

Identity

Package NDC 65219-401-01
Digits Only 6521940101
Product NDC 65219-401
Description

25 VIAL in 1 TRAY (65219-401-01) / 10 mL in 1 VIAL (65219-401-00)

Marketing

Marketing Status
Marketed Since 2022-12-27
Brand zinc sulfate
Generic zinc sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "af258d83-398d-4601-ab09-14c9fe383cc2", "openfda": {"upc": ["0365219403012", "0365219401001", "0365219405023"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["37d54dcd-b720-4168-bfb2-c8f381466aac"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (65219-401-01)  / 10 mL in 1 VIAL (65219-401-00)", "package_ndc": "65219-401-01", "marketing_start_date": "20221227"}], "brand_name": "Zinc Sulfate", "product_id": "65219-401_af258d83-398d-4601-ab09-14c9fe383cc2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "65219-401", "generic_name": "Zinc Sulfate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Sulfate", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA216145", "marketing_category": "ANDA", "marketing_start_date": "20221227", "listing_expiration_date": "20261231"}