Package 67046-1520-3

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1520-3
Digits Only 6704615203
Product NDC 67046-1520
Description

30 TABLET in 1 BLISTER PACK (67046-1520-3)

Marketing

Marketing Status
Marketed Since 2025-02-20
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e96a363-6799-774a-e063-6394a90aac75", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["2e9688ef-781c-aead-e063-6294a90a7bca"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1520-3)", "package_ndc": "67046-1520-3", "marketing_start_date": "20250220"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "67046-1520_2e96a363-6799-774a-e063-6394a90aac75", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "67046-1520", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20250220", "listing_expiration_date": "20261231"}