Package 64380-734-07
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
64380-734-07
Digits Only
6438073407
Product NDC
64380-734
Description
500 TABLET in 1 BOTTLE (64380-734-07)
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": "4ca5f9d2-a4ec-4be1-865f-96a4615087b9", "openfda": {"upc": ["0364380735069", "0364380735083", "0364380736066", "0364380733065", "0364380734086"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["b3d1786d-c3ff-42f1-a09f-37a9c9021e5a"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-734-06)", "package_ndc": "64380-734-06", "marketing_start_date": "20130630"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64380-734-07)", "package_ndc": "64380-734-07", "marketing_start_date": "20130630"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64380-734-08)", "package_ndc": "64380-734-08", "marketing_start_date": "20130630"}], "brand_name": "HydrALAZINE Hydrochloride", "product_id": "64380-734_4ca5f9d2-a4ec-4be1-865f-96a4615087b9", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "64380-734", "generic_name": "HydrALAZINE Hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA200770", "marketing_category": "ANDA", "marketing_start_date": "20130630", "listing_expiration_date": "20261231"}