Package 63187-901-30

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-901-30
Digits Only 6318790130
Product NDC 63187-901
Product ID 63187-901_8abc5903-cbd2-436d-b229-4e76d3726e09
Description

30 TABLET, FILM COATED in 1 BOTTLE (63187-901-30)

Marketing

Marketing Status
Marketed Since 2017-09-01
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": "8abc5903-cbd2-436d-b229-4e76d3726e09", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["63f388e0-9f3d-4902-990c-9a105aa098ad"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-901-30)", "package_ndc": "63187-901-30", "marketing_start_date": "20170901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-901-60)", "package_ndc": "63187-901-60", "marketing_start_date": "20170901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-901-90)", "package_ndc": "63187-901-90", "marketing_start_date": "20170901"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63187-901_8abc5903-cbd2-436d-b229-4e76d3726e09", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63187-901", "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": "25 mg/1"}], "application_number": "ANDA086242", "marketing_category": "ANDA", "marketing_start_date": "20070406", "listing_expiration_date": "20261231"}