Package 0409-4092-01

Brand: copper

Generic: cupric chloride
NDC Package

Package Facts

Identity

Package NDC 0409-4092-01
Digits Only 0409409201
Product NDC 0409-4092
Product ID 0409-4092_6dd188d0-2787-4618-95ba-6a13bfb82e4e
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4092-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4092-11)

Marketing

Marketing Status
Marketed Since 2005-02-28
Brand copper
Generic cupric chloride
Sample Package No

Linked Drug Pages (1)

COPPER ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "6dd188d0-2787-4618-95ba-6a13bfb82e4e", "openfda": {"unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["a84d61a4-8e7f-4be1-aba6-f633b334aafc"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4092-01)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4092-11)", "package_ndc": "0409-4092-01", "marketing_start_date": "20050228"}], "brand_name": "COPPER", "product_id": "0409-4092_6dd188d0-2787-4618-95ba-6a13bfb82e4e", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-4092", "generic_name": "CUPRIC CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COPPER", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "NDA018960", "marketing_category": "NDA", "marketing_start_date": "20050228", "listing_expiration_date": "20261231"}