Package 75834-126-00

Brand: hydralazine

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 75834-126-00
Digits Only 7583412600
Product NDC 75834-126
Description

1000 TABLET in 1 BOTTLE (75834-126-00)

Marketing

Marketing Status
Marketed Since 2017-02-15
Brand hydralazine
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "379fe677-a8e7-4bfe-abcf-85283768c27b", "openfda": {"upc": ["0375834127019", "0375834126012", "0375834128016"], "unii": ["FD171B778Y"], "rxcui": ["905222", "905225", "905395"], "spl_set_id": ["1fd8cf42-66ae-4af5-a5ae-7c9679a0e532"], "manufacturer_name": ["Nivagen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (75834-126-00)", "package_ndc": "75834-126-00", "marketing_start_date": "20170215"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (75834-126-01)", "package_ndc": "75834-126-01", "marketing_start_date": "20170215"}], "brand_name": "Hydralazine", "product_id": "75834-126_379fe677-a8e7-4bfe-abcf-85283768c27b", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "75834-126", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Nivagen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA203845", "marketing_category": "ANDA", "marketing_start_date": "20170215", "listing_expiration_date": "20261231"}