Package 60505-6261-5
Brand: zinc sulfate
Generic: zinc sulfate injectionPackage Facts
Identity
Package NDC
60505-6261-5
Digits Only
6050562615
Product NDC
60505-6261
Description
25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0)
Marketing
Marketing Status
Brand
zinc sulfate
Generic
zinc sulfate injection
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c78f555b-3f22-d031-b241-769f29b4c936", "openfda": {"unii": ["89DS0H96TB"], "rxcui": ["2201524", "2369390"], "spl_set_id": ["b9cf2dab-6ec8-e099-464a-af46a3601971"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0)", "package_ndc": "60505-6261-5", "marketing_start_date": "20250115"}], "brand_name": "Zinc Sulfate", "product_id": "60505-6261_c78f555b-3f22-d031-b241-769f29b4c936", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60505-6261", "generic_name": "Zinc Sulfate Injection", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Sulfate", "active_ingredients": [{"name": "ZINC SULFATE, UNSPECIFIED FORM", "strength": "1 mg/mL"}], "application_number": "ANDA218059", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}