Package 42571-265-75

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 42571-265-75
Digits Only 4257126575
Product NDC 42571-265
Product ID 42571-265_2e500795-07a7-f0f7-e063-6294a90a4e8a
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2017-12-30
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": "2e500795-07a7-f0f7-e063-6294a90a4e8a", "openfda": {"upc": ["0342571265755"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["5a599880-c133-44ef-a9f2-bd1b681563be"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "42571-265-75", "marketing_start_date": "20171230"}], "brand_name": "SODIUM NITROPRUSSIDE", "product_id": "42571-265_2e500795-07a7-f0f7-e063-6294a90a4e8a", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "42571-265", "generic_name": "SODIUM NITROPRUSSIDE", "labeler_name": "Micro Labs Limited", "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": "20171230", "listing_expiration_date": "20261231"}