Package 72819-234-16

Brand: cupric chloride

Generic: cupric chloride
NDC Package

Package Facts

Identity

Package NDC 72819-234-16
Digits Only 7281923416
Product NDC 72819-234
Product ID 72819-234_2472ecab-62ab-84e2-e063-6394a90a86c5
Description

25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-06)

Marketing

Marketing Status
Marketed Since 2024-07-05
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": "2472ecab-62ab-84e2-e063-6394a90a86c5", "openfda": {"upc": ["0372819234168"], "unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["77e9dd68-baed-4d62-9284-daecd995de2c"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-16)  / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-06)", "package_ndc": "72819-234-16", "marketing_start_date": "20240705"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "72819-234_2472ecab-62ab-84e2-e063-6394a90a86c5", "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": "20240705", "listing_expiration_date": "20261231"}