cupric chloride

Generic: cupric chloride

Labeler: archis pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cupric chloride
Generic Name cupric chloride
Labeler archis pharma llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cupric chloride .4 mg/mL

Manufacturer
Archis Pharma LLC

Identifiers & Regulatory

Product NDC 72819-234
Product ID 72819-234_249680fd-f7e7-6e1a-e063-6394a90a87e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217626
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72819234
Hyphenated Format 72819-234

Supplemental Identifiers

RxCUI
204536
UPC
0372819234991
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 cupric chloride (source: ndc)
Generic Name cupric chloride (source: ndc)
Application Number ANDA217626 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96)
source: ndc

Packages (1)

72819-234-99 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96)

Ingredients (1)

cupric chloride (.4 mg/mL)

Linked Drug Pages (2)

CUPRIC CHLORIDE ndc-match (0.9) CUPRIC CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "249680fd-f7e7-6e1a-e063-6394a90a87e7", "openfda": {"upc": ["0372819234991"], "unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["45586a5f-4864-4b01-9211-002c77585249"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99)  / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96)", "package_ndc": "72819-234-99", "marketing_start_date": "20241001"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "72819-234_249680fd-f7e7-6e1a-e063-6394a90a87e7", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "72819-234", "generic_name": "CUPRIC CHLORIDE", "labeler_name": "Archis Pharma 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"}