Package 71205-072-30

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-072-30
Digits Only 7120507230
Product NDC 71205-072
Description

30 TABLET in 1 BOTTLE (71205-072-30)

Marketing

Marketing Status
Marketed Since 2018-07-02
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5696b87a-c388-4cd2-b22b-b2861c28d800", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["dfd60a79-2a30-41e6-b000-a144730099a8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-072-30)", "package_ndc": "71205-072-30", "marketing_start_date": "20180702"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-072-60)", "package_ndc": "71205-072-60", "marketing_start_date": "20180702"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-072-90)", "package_ndc": "71205-072-90", "marketing_start_date": "20180702"}], "brand_name": "HydrALAZINE Hydrochloride", "product_id": "71205-072_5696b87a-c388-4cd2-b22b-b2861c28d800", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71205-072", "generic_name": "HydrALAZINE Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA200770", "marketing_category": "ANDA", "marketing_start_date": "20130630", "listing_expiration_date": "20261231"}