Package 70069-506-25

Brand: cupric chloride

Generic: cupric chloride
NDC Package

Package Facts

Identity

Package NDC 70069-506-25
Digits Only 7006950625
Product NDC 70069-506
Product ID 70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19
Description

25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)

Marketing

Marketing Status
Marketed Since 2024-05-14
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": "ea32e1b7-7c91-478e-9a8c-85f035431e19", "openfda": {"upc": ["0370069506011"], "unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["361d30f2-3c97-4a6c-b252-7fa864d0a625"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PLASTIC in 1 CARTON (70069-506-25)  / 10 mL in 1 VIAL, PLASTIC (70069-506-01)", "package_ndc": "70069-506-25", "marketing_start_date": "20240514"}], "brand_name": "Cupric Chloride", "product_id": "70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19", "dosage_form": "INJECTION", "product_ndc": "70069-506", "generic_name": "Cupric Chloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cupric Chloride", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA216113", "marketing_category": "ANDA", "marketing_start_date": "20240514", "listing_expiration_date": "20261231"}