Package 67457-999-02

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 67457-999-02
Digits Only 6745799902
Product NDC 67457-999
Product ID 67457-999_d94f852b-f928-4e74-b01d-3f69fbe9e5ab
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (67457-999-02) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Discontinued 2027-08-31
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": "d94f852b-f928-4e74-b01d-3f69fbe9e5ab", "openfda": {"upc": ["0367457999029"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["a8999285-16b1-473d-8e92-684f581534f6"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67457-999-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67457-999-02", "marketing_end_date": "20270831", "marketing_start_date": "20201005"}], "brand_name": "Sodium nitroprusside", "product_id": "67457-999_d94f852b-f928-4e74-b01d-3f69fbe9e5ab", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "67457-999", "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_end_date": "20270831", "marketing_start_date": "20201005"}