Package 55150-320-01

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 55150-320-01
Digits Only 5515032001
Product NDC 55150-320
Product ID 55150-320_41e11afb-5fa4-4212-889d-1092dbd0702a
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (55150-320-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2020-12-10
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": "41e11afb-5fa4-4212-889d-1092dbd0702a", "openfda": {"upc": ["0355150320011"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["41e11afb-5fa4-4212-889d-1092dbd0702a"], "manufacturer_name": ["AuroMedics Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (55150-320-01)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-320-01", "marketing_start_date": "20201210"}], "brand_name": "SODIUM NITROPRUSSIDE", "product_id": "55150-320_41e11afb-5fa4-4212-889d-1092dbd0702a", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "55150-320", "generic_name": "SODIUM NITROPRUSSIDE", "labeler_name": "AuroMedics Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM NITROPRUSSIDE", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA211934", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20261231"}