Package 51754-1006-1

Brand: nipride rtu

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 51754-1006-1
Digits Only 5175410061
Product NDC 51754-1006
Product ID 51754-1006_ed0040fb-c481-4477-8712-00fa6350cd70
Description

1 VIAL in 1 VIAL (51754-1006-1) / 100 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-03-20
Brand nipride rtu
Generic sodium nitroprusside
Sample Package No

Linked Drug Pages (1)

NIPRIDE RTU ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ed0040fb-c481-4477-8712-00fa6350cd70", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["1876368", "1876373", "1999185", "1999187", "2052423", "2052424"], "spl_set_id": ["5acf0836-93ff-4064-b888-3f560e8a558d"], "manufacturer_name": ["EXELA PHARMA SCIENCES, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 VIAL (51754-1006-1)  / 100 mL in 1 VIAL", "package_ndc": "51754-1006-1", "marketing_start_date": "20170320"}], "brand_name": "NIPRIDE RTU", "product_id": "51754-1006_ed0040fb-c481-4477-8712-00fa6350cd70", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "51754-1006", "generic_name": "Sodium Nitroprusside", "labeler_name": "EXELA PHARMA SCIENCES, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NIPRIDE RTU", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": ".5 mg/mL"}], "application_number": "NDA209387", "marketing_category": "NDA", "marketing_start_date": "20170320", "listing_expiration_date": "20261231"}