Package 82804-081-90

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-081-90
Digits Only 8280408190
Product NDC 82804-081
Description

90 TABLET in 1 BOTTLE (82804-081-90)

Marketing

Marketing Status
Marketed Since 2024-03-07
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": "004f0059-4ede-4748-9489-45e27c177424", "openfda": {"upc": ["0382804081301"], "unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["024ac6b8-5ce0-4435-9b11-b1806c511d7b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-081-30)", "package_ndc": "82804-081-30", "marketing_start_date": "20240307"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-081-60)", "package_ndc": "82804-081-60", "marketing_start_date": "20240307"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-081-72)", "package_ndc": "82804-081-72", "marketing_start_date": "20250718"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-081-90)", "package_ndc": "82804-081-90", "marketing_start_date": "20240307"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "82804-081_004f0059-4ede-4748-9489-45e27c177424", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "82804-081", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040858", "marketing_category": "ANDA", "marketing_start_date": "20230802", "listing_expiration_date": "20261231"}