Package 51079-074-20

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-074-20
Digits Only 5107907420
Product NDC 51079-074
Description

100 BLISTER PACK in 1 CARTON (51079-074-20) / 1 TABLET in 1 BLISTER PACK (51079-074-01)

Marketing

Marketing Status
Marketed Since 2007-12-26
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": "3a8625af-ede6-2b68-e063-6394a90a4536", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905199", "905225", "905395"], "spl_set_id": ["493a8b7e-5bb1-4db2-91a7-77ed87864131"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-074-20)  / 1 TABLET in 1 BLISTER PACK (51079-074-01)", "package_ndc": "51079-074-20", "marketing_start_date": "20071226"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "51079-074_3a8625af-ede6-2b68-e063-6394a90a4536", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51079-074", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA089097", "marketing_category": "ANDA", "marketing_start_date": "20071226", "listing_expiration_date": "20261231"}