Package 43353-205-05

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43353-205-05
Digits Only 4335320505
Product NDC 43353-205
Product ID 43353-205_7ff2351c-0271-49c1-b5d4-cb73b76a508c
Description

4200 TABLET in 1 BOTTLE (43353-205-05)

Marketing

Marketing Status
Marketed Since 2016-07-09
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": "7ff2351c-0271-49c1-b5d4-cb73b76a508c", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["921c8693-84c2-4313-a2a6-ab3be637d554"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "4200 TABLET in 1 BOTTLE (43353-205-05)", "package_ndc": "43353-205-05", "marketing_start_date": "20160709"}], "brand_name": "HydrALAZINE Hydrochloride", "product_id": "43353-205_7ff2351c-0271-49c1-b5d4-cb73b76a508c", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "43353-205", "generic_name": "HydrALAZINE Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA090255", "marketing_category": "ANDA", "marketing_start_date": "20160520", "listing_expiration_date": "20261231"}