Package 72485-105-01

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 72485-105-01
Digits Only 7248510501
Product NDC 72485-105
Product ID 72485-105_e2df76e1-9850-4469-a3c0-43d2a8cfeba3
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72485-105-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2020-03-27
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": "e2df76e1-9850-4469-a3c0-43d2a8cfeba3", "openfda": {"upc": ["0372485105014"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["d3f1276a-5944-48e3-8ff1-19995ffb7ef9"], "manufacturer_name": ["Armas Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72485-105-01)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72485-105-01", "marketing_start_date": "20200327"}], "brand_name": "SODIUM NITROPRUSSIDE", "product_id": "72485-105_e2df76e1-9850-4469-a3c0-43d2a8cfeba3", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "72485-105", "generic_name": "SODIUM NITROPRUSSIDE", "labeler_name": "Armas Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM NITROPRUSSIDE", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA209352", "marketing_category": "ANDA", "marketing_start_date": "20200327", "listing_expiration_date": "20261231"}