Package 70121-1189-1

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 70121-1189-1
Digits Only 7012111891
Product NDC 70121-1189
Product ID 70121-1189_68b15b81-486f-4f89-9f88-9ac103767767
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2017-11-07
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": "68b15b81-486f-4f89-9f88-9ac103767767", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["2fa687a2-10e7-45ae-953a-9d63564c2908"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70121-1189-1", "marketing_start_date": "20171107"}], "brand_name": "Sodium nitroprusside", "product_id": "70121-1189_68b15b81-486f-4f89-9f88-9ac103767767", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70121-1189", "generic_name": "Sodium nitroprusside", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA209493", "marketing_category": "ANDA", "marketing_start_date": "20171107", "listing_expiration_date": "20261231"}