Package 67046-1609-3

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1609-3
Digits Only 6704616093
Product NDC 67046-1609
Product ID 67046-1609_41c023cd-3a20-a16a-e063-6294a90a493e
Description

30 TABLET in 1 BLISTER PACK (67046-1609-3)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "41c023cd-3a20-a16a-e063-6294a90a493e", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["41c019e3-7b07-5f12-e063-6294a90a5365"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1609-3)", "package_ndc": "67046-1609-3", "marketing_start_date": "20251022"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "67046-1609_41c023cd-3a20-a16a-e063-6294a90a493e", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "67046-1609", "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": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}