Package 70069-261-01
Brand: sodium nitroprusside
Generic: sodium nitroprussidePackage Facts
Identity
Package NDC
70069-261-01
Digits Only
7006926101
Product NDC
70069-261
Description
1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL
Marketing
Marketing Status
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": "040ec67b-55ea-41fd-ae73-8d1ef5ca145b", "openfda": {"upc": ["0370069261019"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["2122b9c1-0af4-493b-82cc-63eee02f987f"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL", "package_ndc": "70069-261-01", "marketing_start_date": "20180817"}], "brand_name": "Sodium Nitroprusside", "product_id": "70069-261_040ec67b-55ea-41fd-ae73-8d1ef5ca145b", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70069-261", "generic_name": "Sodium Nitroprusside", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA210882", "marketing_category": "ANDA", "marketing_start_date": "20180817", "listing_expiration_date": "20261231"}