Package 71335-2352-5
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
71335-2352-5
Digits Only
7133523525
Product NDC
71335-2352
Description
100 TABLET in 1 BOTTLE (71335-2352-5)
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": "c500c938-29f9-44a4-ade1-6915016fc952", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905225"], "spl_set_id": ["ff2c4d1e-33ee-40d7-955b-d736f0559f39"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2352-1)", "package_ndc": "71335-2352-1", "marketing_start_date": "20240221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2352-2)", "package_ndc": "71335-2352-2", "marketing_start_date": "20240221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2352-3)", "package_ndc": "71335-2352-3", "marketing_start_date": "20240221"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2352-4)", "package_ndc": "71335-2352-4", "marketing_start_date": "20240221"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2352-5)", "package_ndc": "71335-2352-5", "marketing_start_date": "20240221"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-2352_c500c938-29f9-44a4-ade1-6915016fc952", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-2352", "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": "25 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}