Package 82804-197-30

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-197-30
Digits Only 8280419730
Product NDC 82804-197
Product ID 82804-197_775e99c4-e18d-4648-a0e3-8709950249ff
Description

30 TABLET in 1 BOTTLE (82804-197-30)

Marketing

Marketing Status
Marketed Since 2025-02-19
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": "775e99c4-e18d-4648-a0e3-8709950249ff", "openfda": {"upc": ["0382804197309"], "unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["775e99c4-e18d-4648-a0e3-8709950249ff"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-197-30)", "package_ndc": "82804-197-30", "marketing_start_date": "20250219"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "82804-197_775e99c4-e18d-4648-a0e3-8709950249ff", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "82804-197", "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": "100 mg/1"}], "application_number": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20100101", "listing_expiration_date": "20261231"}