Package 55150-400-25

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-400-25
Digits Only 5515040025
Product NDC 55150-400
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (55150-400-25) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-02-13
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "f725ae73-cab2-4a30-901c-9f8856803f3a", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["e08d8b6c-a184-4dd5-84ef-bac90e4b1c33"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (55150-400-25)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-400-25", "marketing_start_date": "20230213"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "55150-400_f725ae73-cab2-4a30-901c-9f8856803f3a", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "55150-400", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA215147", "marketing_category": "ANDA", "marketing_start_date": "20230213", "listing_expiration_date": "20261231"}