copper

Generic: cupric chloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name copper
Generic Name cupric chloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cupric chloride .4 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4092
Product ID 0409-4092_6dd188d0-2787-4618-95ba-6a13bfb82e4e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018960
Listing Expiration 2026-12-31
Marketing Start 2005-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094092
Hyphenated Format 0409-4092

Supplemental Identifiers

RxCUI
204536
UNII
S2QG84156O

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name copper (source: ndc)
Generic Name cupric chloride (source: ndc)
Application Number NDA018960 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4092-01) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4092-11)
source: ndc

Packages (1)

Ingredients (1)

cupric chloride (.4 mg/mL)

Linked Drug Pages (1)

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"}