Package 14335-131-01

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 14335-131-01
Digits Only 1433513101
Product NDC 14335-131
Product ID 14335-131_1f875458-09fa-7330-e063-6394a90aac33
Description

1 VIAL in 1 CARTON (14335-131-01) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-08-13
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": "1f875458-09fa-7330-e063-6394a90aac33", "openfda": {"upc": ["0314335131019"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["1f875445-f8e4-b097-e063-6294a90ad544"], "manufacturer_name": ["Hainan Poly Pharm. Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (14335-131-01)  / 2 mL in 1 VIAL", "package_ndc": "14335-131-01", "marketing_start_date": "20240813"}], "brand_name": "sodium nitroprusside", "product_id": "14335-131_1f875458-09fa-7330-e063-6394a90aac33", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "14335-131", "generic_name": "sodium nitroprusside", "labeler_name": "Hainan Poly Pharm. Co., Ltd.", "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": "20240813", "listing_expiration_date": "20261231"}