Package 0641-6231-25
Brand: hydralazine hydrochloride
Generic: hydralazine hydrochloridePackage Facts
Identity
Package NDC
0641-6231-25
Digits Only
0641623125
Product NDC
0641-6231
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6231-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0641-6231-01)
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": "e0fe7653-bdb1-42fc-8277-fc07794f85d5", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["3f5f1204-d289-40e9-be84-a29352f64bfb"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6231-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0641-6231-01)", "package_ndc": "0641-6231-25", "marketing_start_date": "20201218"}], "brand_name": "HydrALAZINE hydrochloride", "product_id": "0641-6231_e0fe7653-bdb1-42fc-8277-fc07794f85d5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "0641-6231", "generic_name": "HydrALAZINE hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrALAZINE hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA213667", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}