Package 0143-9642-01

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 0143-9642-01
Digits Only 0143964201
Product NDC 0143-9642
Product ID 0143-9642_c3a41c1b-a9b0-4ad4-83b8-25e56e2c95fe
Description

5 mL in 1 VIAL (0143-9642-01)

Marketing

Marketing Status
Marketed Since 2013-06-03
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

Linked Drug Pages (1)

Zoledronic Acid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c3a41c1b-a9b0-4ad4-83b8-25e56e2c95fe", "openfda": {"unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["784d33fa-0046-42eb-894b-3fc47dcfd4dc"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL (0143-9642-01)", "package_ndc": "0143-9642-01", "marketing_start_date": "20130603"}], "brand_name": "Zoledronic Acid", "product_id": "0143-9642_c3a41c1b-a9b0-4ad4-83b8-25e56e2c95fe", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "0143-9642", "generic_name": "zoledronic acid", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic Acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA202182", "marketing_category": "ANDA", "marketing_start_date": "20130603", "listing_expiration_date": "20261231"}