Package 68001-610-25

Brand: zoledronic acid

Generic: zoledronic acid
NDC Package

Package Facts

Identity

Package NDC 68001-610-25
Digits Only 6800161025
Product NDC 68001-610
Description

1 VIAL, GLASS in 1 CARTON (68001-610-25) / 5 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2024-02-28
Brand zoledronic acid
Generic zoledronic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3cb94fb2-f06f-69fc-e063-6294a90ad7b4", "openfda": {"upc": ["0368001610254"], "unii": ["6XC1PAD3KF"], "rxcui": ["351114"], "spl_set_id": ["f433c13c-dd8c-4dca-834e-a4ecf09d1eab"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (68001-610-25)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "68001-610-25", "marketing_start_date": "20240228"}], "brand_name": "Zoledronic acid", "product_id": "68001-610_3cb94fb2-f06f-69fc-e063-6294a90ad7b4", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68001-610", "generic_name": "Zoledronic acid", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoledronic acid", "active_ingredients": [{"name": "ZOLEDRONIC ACID", "strength": "4 mg/5mL"}], "application_number": "ANDA201783", "marketing_category": "ANDA", "marketing_start_date": "20240228", "listing_expiration_date": "20261231"}