Package 72819-234-99

Brand: cupric chloride

Generic: cupric chloride
NDC Package

Package Facts

Identity

Package NDC 72819-234-99
Digits Only 7281923499
Product NDC 72819-234
Product ID 72819-234_249680fd-f7e7-6e1a-e063-6394a90a87e7
Description

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

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": "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"}