Package 71872-7145-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7145-1
Digits Only 7187271451
Product NDC 71872-7145
Description

1 VIAL, SINGLE-DOSE in 1 BAG (71872-7145-1) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2018-10-04
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fbd8488b-f04e-fc7f-e053-6394a90a38d5", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["7979c865-737d-d999-e053-2a91aa0abc5e"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7145-1)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7145-1", "marketing_start_date": "20181004"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71872-7145_fbd8488b-f04e-fc7f-e053-6394a90a38d5", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71872-7145", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Medical Purchasing Solutions, LLC", "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": "20010905", "listing_expiration_date": "20261231"}