Package 43598-587-23

Brand: sodium nitroprusside

Generic: sodium nitroprusside
NDC Package

Package Facts

Identity

Package NDC 43598-587-23
Digits Only 4359858723
Product NDC 43598-587
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (43598-587-23) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2019-12-17
Brand sodium nitroprusside
Generic sodium nitroprusside
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "367c01f3-9128-7427-1da8-862b4a9b650c", "openfda": {"upc": ["0343598587233"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["5a689f89-3cbd-f9fa-13cc-26063feb9c83"], "manufacturer_name": ["Dr.Reddy's Laboratories Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (43598-587-23)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "43598-587-23", "marketing_start_date": "20191217"}], "brand_name": "Sodium Nitroprusside", "product_id": "43598-587_367c01f3-9128-7427-1da8-862b4a9b650c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "43598-587", "generic_name": "Sodium Nitroprusside", "labeler_name": "Dr.Reddy's Laboratories Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA210114", "marketing_category": "ANDA", "marketing_start_date": "20191217", "listing_expiration_date": "20261231"}