Package 76282-310-01

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76282-310-01
Digits Only 7628231001
Product NDC 76282-310
Product ID 76282-310_f313fc00-1f7a-40ea-9d61-29c4bfba2426
Description

100 TABLET in 1 BOTTLE (76282-310-01)

Marketing

Marketing Status
Marketed Since 2016-05-20
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": "f313fc00-1f7a-40ea-9d61-29c4bfba2426", "openfda": {"upc": ["0376282309019", "0376282310015", "0376282311012", "0376282312019"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["811831f9-a844-463a-874d-fb8407659f0b"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76282-310-01)", "package_ndc": "76282-310-01", "marketing_start_date": "20160520"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76282-310-10)", "package_ndc": "76282-310-10", "marketing_start_date": "20160520"}], "brand_name": "HydrALAZINE Hydrochloride", "product_id": "76282-310_f313fc00-1f7a-40ea-9d61-29c4bfba2426", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "76282-310", "generic_name": "HydrALAZINE Hydrochloride", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA090255", "marketing_category": "ANDA", "marketing_start_date": "20160520", "listing_expiration_date": "20261231"}