Package 67877-292-05

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67877-292-05
Digits Only 6787729205
Product NDC 67877-292
Product ID 67877-292_26a904df-7070-489e-b0e0-67167a817944
Description

500 TABLET in 1 BOTTLE (67877-292-05)

Marketing

Marketing Status
Marketed Since 2010-05-24
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": "26a904df-7070-489e-b0e0-67167a817944", "openfda": {"upc": ["0367877293011"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["e7bfec3d-5222-4a26-8f99-6c2a28e14aa6"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-292-01)", "package_ndc": "67877-292-01", "marketing_start_date": "20100524"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (67877-292-05)", "package_ndc": "67877-292-05", "marketing_start_date": "20100524"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (67877-292-10)", "package_ndc": "67877-292-10", "marketing_start_date": "20100524"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "67877-292_26a904df-7070-489e-b0e0-67167a817944", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "67877-292", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA200737", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}