Package 63629-8493-1
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
63629-8493-1
Digits Only
6362984931
Product NDC
63629-8493
Description
1000 TABLET in 1 BOTTLE (63629-8493-1)
Marketing
Marketing Status
Brand
hydralazine hydrochloride
Generic
hydralazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6cbee232-1810-4489-b081-362d0e41399b", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["4985994c-23ab-4409-bab6-5a17db767f13"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-8493-1)", "package_ndc": "63629-8493-1", "marketing_start_date": "20210518"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "63629-8493_6cbee232-1810-4489-b081-362d0e41399b", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63629-8493", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}