Package 70710-1877-7

Brand: zinc sulfate

Generic: zinc sulfate injection,
NDC Package

Package Facts

Identity

Package NDC 70710-1877-7
Digits Only 7071018777
Product NDC 70710-1877
Description

25 VIAL in 1 CARTON (70710-1877-7) / 10 mL in 1 VIAL (70710-1877-1)

Marketing

Marketing Status
Marketed Since 2023-12-07
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": "245bc553-262e-47ff-91d0-0b7c136b6413", "openfda": {"upc": ["0370710187675"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["95aa8437-10bc-4205-939f-d21d8fa52a00"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70710-1877-7)  / 10 mL in 1 VIAL (70710-1877-1)", "package_ndc": "70710-1877-7", "marketing_start_date": "20231207"}], "brand_name": "zinc sulfate", "product_id": "70710-1877_245bc553-262e-47ff-91d0-0b7c136b6413", "dosage_form": "SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70710-1877", "generic_name": "zinc sulfate injection,", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "zinc sulfate", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "3 mg/mL"}], "application_number": "ANDA217074", "marketing_category": "ANDA", "marketing_start_date": "20231207", "listing_expiration_date": "20261231"}