Package 70518-3659-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3659-1
Digits Only 7051836591
Product NDC 70518-3659
Product ID 70518-3659_3b01d911-7a5c-d4fc-e063-6294a90a57e2
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (70518-3659-1) / 1 mL in 1 VIAL, SINGLE-DOSE (70518-3659-2)

Marketing

Marketing Status
Marketed Since 2024-09-19
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

hydrALAZINE Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3b01d911-7a5c-d4fc-e063-6294a90a57e2", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["dca82025-a4cd-4856-aa19-bdf091bf8973"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (70518-3659-1)  / 1 mL in 1 VIAL, SINGLE-DOSE (70518-3659-2)", "package_ndc": "70518-3659-1", "marketing_start_date": "20240919"}], "brand_name": "hydrALAZINE Hydrochloride", "product_id": "70518-3659_3b01d911-7a5c-d4fc-e063-6294a90a57e2", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "70518-3659", "generic_name": "hydrALAZINE Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040388", "marketing_category": "ANDA", "marketing_start_date": "20230227", "listing_expiration_date": "20261231"}