Package 82868-045-30

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-045-30
Digits Only 8286804530
Product NDC 82868-045
Product ID 82868-045_46dcba1e-2a2e-cfd1-e063-6394a90a19ee
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-045-30)

Marketing

Marketing Status
Marketed Since 2024-02-15
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": "46dcba1e-2a2e-cfd1-e063-6394a90a19ee", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["1275dd50-d97f-2e8f-e063-6394a90a4a67"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-045-30)", "package_ndc": "82868-045-30", "marketing_start_date": "20240215"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "82868-045_46dcba1e-2a2e-cfd1-e063-6394a90a19ee", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "82868-045", "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": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}