Package 51655-916-52

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-916-52
Digits Only 5165591652
Product NDC 51655-916
Product ID 51655-916_4974183f-5839-7ea9-e063-6294a90ad99e
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-916-52)

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": "4974183f-5839-7ea9-e063-6294a90ad99e", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["ada28f78-e933-7acf-e053-2995a90ae316"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-916-26)", "package_ndc": "51655-916-26", "marketing_end_date": "20260831", "marketing_start_date": "20200526"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-916-52)", "package_ndc": "51655-916-52", "marketing_end_date": "20260831", "marketing_start_date": "20230712"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "51655-916_4974183f-5839-7ea9-e063-6294a90ad99e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51655-916", "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": "50 mg/1"}], "application_number": "ANDA086242", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20200526"}