Package 67457-839-02

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 67457-839-02
Digits Only 6745783902
Product NDC 67457-839
Product ID 67457-839_e408516c-5b97-450d-a4b4-d1b07b4f029c
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2018-08-10
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": "e408516c-5b97-450d-a4b4-d1b07b4f029c", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["6fbfb86c-da8d-4741-b1e0-7000e2bbad5f"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67457-839-02", "marketing_start_date": "20180810"}], "brand_name": "Sodium nitroprusside", "product_id": "67457-839_e408516c-5b97-450d-a4b4-d1b07b4f029c", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "67457-839", "generic_name": "Sodium nitroprusside", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA210763", "marketing_category": "ANDA", "marketing_start_date": "20180810", "listing_expiration_date": "20261231"}