Package 70436-207-80

Brand: sodium nitroprusside in 0.9% sodium chloride

Generic: sodium nitroprusside in 0.9% sodium chloride
NDC Package

Package Facts

Identity

Package NDC 70436-207-80
Digits Only 7043620780
Product NDC 70436-207
Product ID 70436-207_09c94d69-7bea-2491-e063-6394a90a6438
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (70436-207-80) / 100 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-31
Brand sodium nitroprusside in 0.9% sodium chloride
Generic sodium nitroprusside in 0.9% sodium chloride
Sample Package No

Linked Drug Pages (1)

sodium nitroprusside in 0.9% sodium chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "09c94d69-7bea-2491-e063-6394a90a6438", "openfda": {"upc": ["0370436206803"], "unii": ["EAO03PE1TC"], "rxcui": ["1876368", "1999185", "2052423"], "spl_set_id": ["6f02e4ac-5f7c-4003-b9b7-283f489cddb0"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70436-207-80)  / 100 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70436-207-80", "marketing_start_date": "20221231"}], "brand_name": "sodium nitroprusside in 0.9% sodium chloride", "product_id": "70436-207_09c94d69-7bea-2491-e063-6394a90a6438", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70436-207", "generic_name": "sodium nitroprusside in 0.9% sodium chloride", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sodium nitroprusside in 0.9% sodium chloride", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA215846", "marketing_category": "ANDA", "marketing_start_date": "20221231", "listing_expiration_date": "20261231"}