Package 0517-0901-25

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0517-0901-25
Digits Only 0517090125
Product NDC 0517-0901
Product ID 0517-0901_5aca9ccd-3ac3-48b6-9372-34ee0eb4b7f9
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 1997-06-30
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5aca9ccd-3ac3-48b6-9372-34ee0eb4b7f9", "openfda": {"upc": ["0305170901257"], "unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["17210abc-58f6-442e-8ff2-7971333c82f6"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0517-0901-25", "marketing_start_date": "19970630"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "0517-0901_5aca9ccd-3ac3-48b6-9372-34ee0eb4b7f9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "0517-0901", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040136", "marketing_category": "ANDA", "marketing_start_date": "19970630", "listing_expiration_date": "20261231"}