Package 31722-453-31

Brand: zinc sulfate

Generic: zinc sulfate
NDC Package

Package Facts

Identity

Package NDC 31722-453-31
Digits Only 3172245331
Product NDC 31722-453
Description

25 VIAL in 1 CARTON (31722-453-31) / 10 mL in 1 VIAL (31722-453-10)

Marketing

Marketing Status
Marketed Since 2025-05-01
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": "4c2fa3c5-612d-9133-e063-6394a90ab707", "openfda": {"upc": ["0331722453103", "0331722455329", "0331722454100"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["49698d00-f44b-4b1f-ae34-6b9067911757"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (31722-453-31)  / 10 mL in 1 VIAL (31722-453-10)", "package_ndc": "31722-453-31", "marketing_start_date": "20250501"}], "brand_name": "ZINC SULFATE", "product_id": "31722-453_4c2fa3c5-612d-9133-e063-6394a90ab707", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "31722-453", "generic_name": "ZINC SULFATE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZINC SULFATE", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA219585", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20271231"}