Package 60505-6260-5

Brand: zinc sulfate

Generic: zinc sulfate injection
NDC Package

Package Facts

Identity

Package NDC 60505-6260-5
Digits Only 6050562605
Product NDC 60505-6260
Description

25 VIAL in 1 CARTON (60505-6260-5) / 5 mL in 1 VIAL (60505-6260-0)

Marketing

Marketing Status
Marketed Since 2024-08-01
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 (60505-6260-5)  / 5 mL in 1 VIAL (60505-6260-0)", "package_ndc": "60505-6260-5", "marketing_start_date": "20240801"}], "brand_name": "Zinc Sulfate", "product_id": "60505-6260_c78f555b-3f22-d031-b241-769f29b4c936", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60505-6260", "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": "5 mg/mL"}], "application_number": "ANDA218059", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}