Package 72572-265-25

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72572-265-25
Digits Only 7257226525
Product NDC 72572-265
Product ID 72572-265_c25506f2-689e-4053-b858-8424e6724ed6
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (72572-265-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72572-265-01)

Marketing

Marketing Status
Marketed Since 2020-10-29
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": "c25506f2-689e-4053-b858-8424e6724ed6", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["ffa483a4-de2a-4d42-ad27-afacd37f28e4"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (72572-265-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (72572-265-01)", "package_ndc": "72572-265-25", "marketing_start_date": "20201029"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "72572-265_c25506f2-689e-4053-b858-8424e6724ed6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72572-265", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040136", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20261231"}