Package 67046-1517-3

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1517-3
Digits Only 6704615173
Product NDC 67046-1517
Product ID 67046-1517_2df48c89-03d8-aa07-e063-6394a90acb7e
Description

30 TABLET in 1 BLISTER PACK (67046-1517-3)

Marketing

Marketing Status
Marketed Since 2025-02-12
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": "2df48c89-03d8-aa07-e063-6394a90acb7e", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["2df51a19-a39a-0ec8-e063-6394a90a147c"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1517-3)", "package_ndc": "67046-1517-3", "marketing_start_date": "20250212"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "67046-1517_2df48c89-03d8-aa07-e063-6394a90acb7e", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "67046-1517", "generic_name": "hydralazine hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203845", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}