Package 50090-6608-0

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6608-0
Digits Only 5009066080
Product NDC 50090-6608
Product ID 50090-6608_29ea9739-73f0-4dc5-9392-8088957cb30c
Description

90 TABLET in 1 BOTTLE (50090-6608-0)

Marketing

Marketing Status
Marketed Since 2023-08-22
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29ea9739-73f0-4dc5-9392-8088957cb30c", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["e617023e-b060-4db9-a97e-e2b11a37901e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6608-0)", "package_ndc": "50090-6608-0", "marketing_start_date": "20230822"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "50090-6608_29ea9739-73f0-4dc5-9392-8088957cb30c", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "50090-6608", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA088468", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}