Package 63323-614-55
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
63323-614-55
Digits Only
6332361455
Product NDC
63323-614
Description
25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-21)
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": "2f8362b3-0a39-40b0-95bf-4a786cb15a74", "openfda": {"upc": ["0363323614218"], "unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["c3797028-c625-4f70-ae69-8a5f6f23f1b8"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-21)", "package_ndc": "63323-614-55", "marketing_start_date": "20110131"}], "brand_name": "hydrALAZINE Hydrochloride", "product_id": "63323-614_2f8362b3-0a39-40b0-95bf-4a786cb15a74", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "63323-614", "generic_name": "hydrALAZINE Hydrochloride", "labeler_name": "Fresenius Kabi USA, 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": "20110131", "listing_expiration_date": "20261231"}