Package 71839-120-01

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 71839-120-01
Digits Only 7183912001
Product NDC 71839-120
Product ID 71839-120_01841345-bed3-458f-8e99-911fbd286512
Description

1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-07-12
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": "01841345-bed3-458f-8e99-911fbd286512", "openfda": {"upc": ["0371839120017"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["01841345-bed3-458f-8e99-911fbd286512"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (71839-120-01)  / 2 mL in 1 VIAL", "package_ndc": "71839-120-01", "marketing_start_date": "20210712"}], "brand_name": "Sodium Nitroprusside", "product_id": "71839-120_01841345-bed3-458f-8e99-911fbd286512", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "71839-120", "generic_name": "Sodium Nitroprusside", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA214971", "marketing_category": "ANDA", "marketing_start_date": "20210712", "listing_expiration_date": "20261231"}