Package 51662-1376-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1376-1
Digits Only 5166213761
Product NDC 51662-1376
Description

1 mL in 1 VIAL, SINGLE-DOSE (51662-1376-1)

Marketing

Marketing Status
Marketed Since 2019-12-09
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": "103515bd-ec41-5646-e063-6394a90ae3b4", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["9949407f-e410-7f47-e053-2995a90a7369"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1376-1)", "package_ndc": "51662-1376-1", "marketing_start_date": "20191209"}, {"sample": false, "description": "25 POUCH in 1 BOX (51662-1376-3)  / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1376-2)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1376-3", "marketing_start_date": "20210511"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "51662-1376_103515bd-ec41-5646-e063-6394a90ae3b4", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51662-1376", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20191209", "listing_expiration_date": "20261231"}