Package 72603-351-25

Brand: cupric chloride

Generic: cupric chloride
NDC Package

Package Facts

Identity

Package NDC 72603-351-25
Digits Only 7260335125
Product NDC 72603-351
Product ID 72603-351_23070470-7866-f913-e063-6394a90add5f
Description

25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01)

Marketing

Marketing Status
Marketed Since 2024-10-01
Brand cupric chloride
Generic cupric chloride
Sample Package No

Linked Drug Pages (1)

CUPRIC CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "23070470-7866-f913-e063-6394a90add5f", "openfda": {"upc": ["0372603351255"], "unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["db988413-2998-4fc0-bcdf-11076256bf6e"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25)  / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01)", "package_ndc": "72603-351-25", "marketing_start_date": "20241001"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "72603-351_23070470-7866-f913-e063-6394a90add5f", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "72603-351", "generic_name": "CUPRIC CHLORIDE", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CUPRIC CHLORIDE", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA217626", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}