Package 68788-8087-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8087-1
Digits Only 6878880871
Product NDC 68788-8087
Product ID 68788-8087_25ed7d1a-86d6-41b4-9a75-0fb5af3aeabb
Description

100 TABLET in 1 BOTTLE (68788-8087-1)

Marketing

Marketing Status
Marketed Since 2021-10-05
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": "25ed7d1a-86d6-41b4-9a75-0fb5af3aeabb", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905222"], "spl_set_id": ["438479d0-ff61-4008-a0fc-1ee44b97cf7f"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8087-1)", "package_ndc": "68788-8087-1", "marketing_start_date": "20211005"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "68788-8087_25ed7d1a-86d6-41b4-9a75-0fb5af3aeabb", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68788-8087", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20211005", "listing_expiration_date": "20261231"}