Package 43063-392-90

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-392-90
Digits Only 4306339290
Product NDC 43063-392
Product ID 43063-392_47d22c09-1a2d-02c7-e063-6294a90a3005
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-392-90)

Marketing

Marketing Status
Marketed Since 2011-03-15
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

HYDRALAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d22c09-1a2d-02c7-e063-6294a90a3005", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["e9450e82-329f-4fd8-a0b3-3e8e22715965"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-392-90)", "package_ndc": "43063-392-90", "marketing_start_date": "20110315"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "43063-392_47d22c09-1a2d-02c7-e063-6294a90a3005", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "43063-392", "generic_name": "hydralazine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA086242", "marketing_category": "ANDA", "marketing_start_date": "20070406", "listing_expiration_date": "20271231"}