Package 51655-305-83

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-305-83
Digits Only 5165530583
Product NDC 51655-305
Product ID 51655-305_48eaeb02-b2f5-5a36-e063-6394a90ac5e9
Description

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-305-83)

Marketing

Marketing Status
Discontinued 2026-08-31
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": "48eaeb02-b2f5-5a36-e063-6394a90ac5e9", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["ab1c6f37-3b64-23fb-e053-2995a90a932f"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-305-26)", "package_ndc": "51655-305-26", "marketing_end_date": "20260831", "marketing_start_date": "20200520"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-305-83)", "package_ndc": "51655-305-83", "marketing_end_date": "20260831", "marketing_start_date": "20200528"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "51655-305_48eaeb02-b2f5-5a36-e063-6394a90ac5e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51655-305", "generic_name": "hydralazine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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_end_date": "20260831", "marketing_start_date": "20200520"}