Package 84549-614-55

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-614-55
Digits Only 8454961455
Product NDC 84549-614
Product ID 84549-614_3a38e0e3-de87-9cb7-e063-6294a90a60ba
Description

1 mL in 1 VIAL, SINGLE-DOSE (84549-614-55)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "3a38e0e3-de87-9cb7-e063-6294a90a60ba", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["3855c3da-ff25-8301-e063-6294a90a22b3"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-614-55)", "package_ndc": "84549-614-55", "marketing_start_date": "20250827"}], "brand_name": "hydrALAZINE Hydrochloride", "product_id": "84549-614_3a38e0e3-de87-9cb7-e063-6294a90a60ba", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "84549-614", "generic_name": "hydrALAZINE Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydrALAZINE Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040388", "marketing_category": "ANDA", "marketing_start_date": "20110131", "listing_expiration_date": "20261231"}