Package 71288-202-02

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 71288-202-02
Digits Only 7128820202
Product NDC 71288-202
Product ID 71288-202_e5bd8841-49d6-43fd-9c13-5d0134872ce2
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2019-12-06
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": "e5bd8841-49d6-43fd-9c13-5d0134872ce2", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["820eadcb-1230-4b17-a652-e69b52b3c12f"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-202-02", "marketing_start_date": "20191206"}], "brand_name": "Sodium Nitroprusside", "product_id": "71288-202_e5bd8841-49d6-43fd-9c13-5d0134872ce2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "71288-202", "generic_name": "Sodium Nitroprusside", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA211016", "marketing_category": "ANDA", "marketing_start_date": "20191206", "listing_expiration_date": "20261231"}