Package 55289-133-60

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55289-133-60
Digits Only 5528913360
Product NDC 55289-133
Product ID 55289-133_47e36800-0665-cf64-e063-6294a90a85af
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-133-60)

Marketing

Marketing Status
Marketed Since 2022-06-24
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": "47e36800-0665-cf64-e063-6294a90a85af", "openfda": {"upc": ["0355289133605"], "unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["4671cefa-4468-4116-ba40-3d3b0f581ea1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-133-60)", "package_ndc": "55289-133-60", "marketing_start_date": "20220624"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "55289-133_47e36800-0665-cf64-e063-6294a90a85af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "55289-133", "generic_name": "hydralazine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20271231"}