Package 67046-1520-3
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage 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
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"}