Package 70436-028-80

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 70436-028-80
Digits Only 7043602880
Product NDC 70436-028
Product ID 70436-028_b17353da-2c56-d579-e053-2995a90a8227
Description

1 VIAL in 1 CARTON (70436-028-80) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-10-15
Brand sodium nitroprusside
Generic sodium nitroprusside
Sample Package No

Linked Drug Pages (1)

sodium nitroprusside ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b17353da-2c56-d579-e053-2995a90a8227", "openfda": {"upc": ["0370436028801"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["01dfae56-3d9b-448a-84a7-03a54a533eb1"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70436-028-80)  / 2 mL in 1 VIAL", "package_ndc": "70436-028-80", "marketing_start_date": "20201015"}], "brand_name": "sodium nitroprusside", "product_id": "70436-028_b17353da-2c56-d579-e053-2995a90a8227", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70436-028", "generic_name": "sodium nitroprusside", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sodium nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA214199", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}