Package 71872-7145-1
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
71872-7145-1
Digits Only
7187271451
Product NDC
71872-7145
Description
1 VIAL, SINGLE-DOSE in 1 BAG (71872-7145-1) / 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": "fbd8488b-f04e-fc7f-e053-6394a90a38d5", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["7979c865-737d-d999-e053-2a91aa0abc5e"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7145-1) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7145-1", "marketing_start_date": "20181004"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71872-7145_fbd8488b-f04e-fc7f-e053-6394a90a38d5", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71872-7145", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "Medical Purchasing Solutions, LLC", "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": "20010905", "listing_expiration_date": "20261231"}