Package 51754-0103-4
Brand: cupric chloride
Generic: cupric chloridePackage Facts
Identity
Package NDC
51754-0103-4
Digits Only
5175401034
Product NDC
51754-0103
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
cupric chloride
Generic
cupric chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "18dc9e1c-b9db-4160-96f7-8c4391bcf8c9", "openfda": {"unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["daaa6f3a-148e-4f1c-bd44-bb2242145b88"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51754-0103-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51754-0103-4", "marketing_start_date": "20230201"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "51754-0103_18dc9e1c-b9db-4160-96f7-8c4391bcf8c9", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51754-0103", "generic_name": "cupric chloride", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CUPRIC CHLORIDE", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA212071", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}