Package 51662-1648-3
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
51662-1648-3
Digits Only
5166216483
Product NDC
51662-1648
Description
25 POUCH in 1 CASE (51662-1648-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1648-2) / 1 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
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": "15b1adc3-9cb5-cf06-e063-6294a90a1da7", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["15b0f03b-b5a2-c49d-e063-6394a90a5b15"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1648-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1648-2) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1648-3", "marketing_start_date": "19970630"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "51662-1648_15b1adc3-9cb5-cf06-e063-6294a90a1da7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51662-1648", "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": "ANDA040136", "marketing_category": "ANDA", "marketing_start_date": "19970630", "listing_expiration_date": "20261231"}