Package 72162-1537-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1537-0
Digits Only 7216215370
Product NDC 72162-1537
Product ID 72162-1537_8ac9ca78-3c6b-4fe6-9a30-2d4e313a8dda
Description

1000 TABLET in 1 BOTTLE (72162-1537-0)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": ["ORAL"], "spl_id": "8ac9ca78-3c6b-4fe6-9a30-2d4e313a8dda", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["d5b0165e-9823-470a-8ed0-5c4c8722369d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1537-0)", "package_ndc": "72162-1537-0", "marketing_start_date": "20240205"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "72162-1537_8ac9ca78-3c6b-4fe6-9a30-2d4e313a8dda", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72162-1537", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}