Package 71335-2307-3
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
71335-2307-3
Digits Only
7133523073
Product NDC
71335-2307
Description
90 TABLET in 1 BOTTLE (71335-2307-3)
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": "f30b02c3-4e14-4cbd-98d2-4d04e00c77f8", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199"], "spl_set_id": ["914d5b62-6f9b-4665-8562-689367c36230"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2307-1)", "package_ndc": "71335-2307-1", "marketing_start_date": "20231214"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2307-2)", "package_ndc": "71335-2307-2", "marketing_start_date": "20231214"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2307-3)", "package_ndc": "71335-2307-3", "marketing_start_date": "20231214"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2307-4)", "package_ndc": "71335-2307-4", "marketing_start_date": "20231214"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-2307_f30b02c3-4e14-4cbd-98d2-4d04e00c77f8", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-2307", "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"}