Package 0904-7450-61

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7450-61
Digits Only 0904745061
Product NDC 0904-7450
Product ID 0904-7450_73a8ca83-9f63-4264-b36f-e133d98d5002
Description

100 BLISTER PACK in 1 CARTON (0904-7450-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-03
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": "73a8ca83-9f63-4264-b36f-e133d98d5002", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["b6ccd35e-f69c-4eef-a456-905e030ae911"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7450-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7450-61", "marketing_start_date": "20250103"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "0904-7450_73a8ca83-9f63-4264-b36f-e133d98d5002", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "0904-7450", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20250103", "listing_expiration_date": "20261231"}