Package 68083-608-25

Brand: zinc sulfate

Generic: zinc sulfate
NDC Package

Package Facts

Identity

Package NDC 68083-608-25
Digits Only 6808360825
Product NDC 68083-608
Description

25 VIAL in 1 CARTON (68083-608-25) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-09-01
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": "cfa59996-1de2-4313-a7ac-1766764513e2", "openfda": {"unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["8f354f0a-4e10-4e4e-b86c-49d97cbd631d"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (68083-608-25)  / 10 mL in 1 VIAL", "package_ndc": "68083-608-25", "marketing_start_date": "20230901"}], "brand_name": "Zinc Sulfate", "product_id": "68083-608_cfa59996-1de2-4313-a7ac-1766764513e2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "68083-608", "generic_name": "Zinc Sulfate", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Sulfate", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA216249", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}